TWI337915B - Backingless abrasive article - Google Patents

Backingless abrasive article Download PDF

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Publication number
TWI337915B
TWI337915B TW096125711A TW96125711A TWI337915B TW I337915 B TWI337915 B TW I337915B TW 096125711 A TW096125711 A TW 096125711A TW 96125711 A TW96125711 A TW 96125711A TW I337915 B TWI337915 B TW I337915B
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TW
Taiwan
Prior art keywords
abrasive article
abrasive
layer
formulation
particles
Prior art date
Application number
TW096125711A
Other languages
Chinese (zh)
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TW200812755A (en
Inventor
Ramaswamy Sankaranarayanan
Original Assignee
Saint Gobain Abrasives Inc
Saint Gobain Abrasifs Sa
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Publication of TW200812755A publication Critical patent/TW200812755A/en
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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/02Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent
    • B24D3/20Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially organic
    • B24D3/22Rubbers synthetic or natural
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D11/00Constructional features of flexible abrasive materials; Special features in the manufacture of such materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D11/00Constructional features of flexible abrasive materials; Special features in the manufacture of such materials
    • B24D11/001Manufacture of flexible abrasive materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D18/00Manufacture of grinding tools or other grinding devices, e.g. wheels, not otherwise provided for
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/001Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as supporting member
    • B24D3/002Flexible supporting members, e.g. paper, woven, plastic materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/02Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent
    • B24D3/20Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially organic

Description

九、發明說明: 【發明所屬之技術領域】 叙月大肋_而s係關於無背層部件之研磨物件。 【先前技術】 諸里土佈研磨物件及黏合研磨物件之研磨物件用於各 種產業中用以(諸如)藉由精磨、研磨或拋光來加工工件。 寿J用研磨物件進仃加工橫跨自一般修整及材料移除產業應 用至光學產業及汽車補漆業至金屬製造業的廣泛產業範 V °在此等實例之各者中’製造促進使用研磨劑移除塊狀 材料或影響產品之表面特性。 表面特性包括光澤、紋理及均一性。詳言之,表面特性 (諸如粗糙度及光澤)可影響光學媒體之效能。光學媒體正 越來越多地用於資料儲存,特別是包括遊戲、圖片 '電影 及音樂之數位娛樂資料。表面刮痕或不良表面品質可能在 光學媒體存取時引入錯誤,且在許多狀況下可能使得光學 媒體不能讀取或不能播放。特別是在光學媒體被頻繁再使 用或轉售的情形下’需要表面修復。 表面特性亦可影響汽車補漆之品質.舉例而言,當對表 面塗漆時,油漆通常係噴塗在表面上並固化。所得塗漆表 面具有麻窩狀橘皮紋理或包括包袠灰塵缺陷。通常,首先 用粗粒研磨劑打磨塗漆表面,且隨後用細粒工程研磨劑打 磨且用羊毛墊或發泡體墊磨光。 除表面特性外,諸如光學媒體租賃及轉售業或汽車塗漆 業之產業對成本敏感。影響運作成本之因素包括處理2 122813.doc 1337915 之速度及用於處理該表面之材料之成本。通常,產業尋求 具有較高材料移除速率之具有成本效益之材料。 然而’展現較高移除速率之研磨劑在達成理想表面特性 方面常展現不良效能。相反,產生理想表面特性之研磨劑 #具有較低材料移除速率。為此,表面處理常為使用各種 f級之研磨板之多步驟過程。通常,在後續步驟中使用細 粒研磨劑修復由單步操作所引入之表面瑕疵。由此,引入 '細微刮痕及表面瑕疫之研磨劑導致後續步驟中付出之勞動 增加。 通*任步驟中勞動之任何增加均#致成本增加。舉 例而。勞動〜加包括用於改良表面品質之時間增加及在 •該步驟期間所使用之研磨產品之數目增加。時間增加及步 驟中所使用之研磨產品之數目增加均導致成本增加,從而 導致在市場中之劣勢。 CD、DVD及遊戲轉售商店及租f提供者較佳在後續租 • f或銷售之前進行光學媒體之單步表面修復。因此,需要 自使用早-研磨產品同時獲得高移除速率及高品質表面特 性。不良品質表面特性可降低表面修復之成功率,且因此 或㈣之收入損失及與__之重新μ㈣ 之花費。另一方面,低移除率導致低產量及低效率。 因此’需要-種在使用時提供經改良之表面特性的具有 成本效益之工程研磨物件。 【發明内容】 在特疋實施例中’研磨物件包括具有一列突起之研磨 I22813.doc 研磨物件無背 層。研磨層具有不大於約100密耳之厚度 層。 在另一例示性實施例中,研磨物件包括具有第—主表面 及第二主表面之研磨層。第一主表面界定一組自研磨物件 之第一表面伸出之突起。研磨物件包括直接與第二主表面 接觸之黏著層。黏著層界定研磨物件之第二表面。 在另一例示性實施例中,研磨物件包括具有第一主表面 及第二主表面之研磨層。第一主表面界定一組突起。研磨 物件亦包括直接與第二主表面接觸之黏著層且包括直接與 黏著層接觸之扣件層。 在一特定實施例中,研磨物件係由固化調配物形成。該 調配物包括液體聚矽氧橡膠、二氧化矽增強顆粒及研= 粒。 在另一例示性實施例中,一種方法包括摻合液體聚矽氧 橡膠、二氧化矽增強顆粒及研磨粒以形成調配物。該方法 進一步包括由調配物形成表面特徵層及使調配物固化。 在另一例示性實施例中,研磨物件包括包含聚矽氧黏合 劑及研磨粒之層β該層具有至少約50%之伸長率。 在另一例示性實施例中,研磨物件包括經組態成表面積 隨著磨損而增加之表面特徵層。表面特徵層包括聚矽氧黏 合劑及研磨粒。表面特徵層具有不大於約500密耳之厚 度。研磨物件無背層。 在另一例示性實施例中,研磨物件包括具有表面突起之 層。該層包括聚石夕氧點合劑及研磨哲。研磨物件具有至少 122813.doc 1337915 約20之光澤效能。 在一額外實施例中,一種修整塗漆表面之方法包括用由 固化調配物形成之研磨物件研磨塗漆表面。該調配物包括 液體聚矽氧橡膠、二氧化矽增強顆粒及研磨粒。該方法進 一步包括拋光經研磨之塗漆表面。 在另一例示性實施例中,一種修整塗漆表面之方法包括 用研磨物件研磨塗漆表面,該研磨物件包括經組態成表面 積隨著磨損而增加之表面特徵層。該層包括聚矽氧黏合劑 及研磨粒。研磨物件無背層。該方法進一步包括拋光經研 磨之塗漆表面。 【實施方式】Nine, the invention description: [Technical field to which the invention pertains] The ribs of the invention are related to the abrasive articles of the non-back layer components. [Prior Art] Aboriginal abrasive articles and abrasive articles bonded to abrasive articles are used in various industries for processing workpieces, such as by grinding, grinding or polishing. Shou J uses abrasive articles to process a wide range of industries from general trimming and material removal industry applications to the optical industry and automotive refinishing industry to metal manufacturing. V ° In each of these examples, 'manufacturing promotes the use of grinding The agent removes the bulk material or affects the surface properties of the product. Surface properties include gloss, texture and uniformity. In particular, surface characteristics such as roughness and gloss can affect the performance of optical media. Optical media is increasingly being used for data storage, especially for games, movies, and digital entertainment. Surface scratches or poor surface quality can introduce errors in optical media access and, in many cases, can cause optical media to be unreadable or unplayable. Especially in the case where optical media are frequently reused or resold, surface repair is required. Surface properties can also affect the quality of automotive touch up paint. For example, when painting a surface, the paint is typically sprayed onto the surface and cured. The resulting painted surface has a linen-like orange peel texture or includes a dusty defect. Typically, the painted surface is first sanded with a coarse abrasive and then sanded with a fine grain engineering abrasive and buffed with a wool pad or foam pad. In addition to surface characteristics, industries such as optical media leasing and resale or automotive paint industries are cost sensitive. Factors affecting operating costs include the speed of processing 2 122813.doc 1337915 and the cost of materials used to treat the surface. Often, the industry seeks cost effective materials with higher material removal rates. However, abrasives exhibiting higher removal rates often exhibit poor performance in achieving the desired surface characteristics. In contrast, abrasive #, which produces the desired surface characteristics, has a lower material removal rate. For this reason, surface treatment is often a multi-step process using a variety of grade f abrasive plates. Typically, fine abrasives are used in subsequent steps to repair surface imperfections introduced by single-step operations. Thus, the introduction of 'fine scratches and surface plague abrasives leads to increased labor in subsequent steps. Any increase in labor in the pass-through step #increased cost increase. For example. Labor ~ plus includes an increase in the time for improving the surface quality and an increase in the number of abrasive products used during the step. The increase in time and the increase in the number of abrasive products used in the steps lead to increased costs, which leads to disadvantages in the market. CD, DVD and game resale stores and rental providers are better able to perform single-step surface repair of optical media prior to subsequent rental or sales. Therefore, it is necessary to obtain high removal rates and high quality surface characteristics from the use of early-grinding products. Poor quality surface characteristics can reduce the success rate of surface repair, and therefore or (4) the loss of revenue and the cost of re-μ (4) with __. On the other hand, low removal rates result in low throughput and low efficiency. Therefore, it is desirable to have a cost-effective engineered abrasive article that provides improved surface characteristics when in use. SUMMARY OF THE INVENTION In a particular embodiment, the abrasive article comprises a polishing I22813.doc abrasive article having an array of protrusions without a backing. The abrasive layer has a thickness layer of no greater than about 100 mils. In another exemplary embodiment, the abrasive article includes an abrasive layer having a first major surface and a second major surface. The first major surface defines a plurality of projections extending from the first surface of the abrasive article. The abrasive article includes an adhesive layer that is in direct contact with the second major surface. The adhesive layer defines a second surface of the abrasive article. In another exemplary embodiment, an abrasive article includes an abrasive layer having a first major surface and a second major surface. The first major surface defines a set of protrusions. The abrasive article also includes an adhesive layer that is in direct contact with the second major surface and includes a fastener layer that is in direct contact with the adhesive layer. In a particular embodiment, the abrasive article is formed from a cured formulation. The formulation includes a liquid polyoxyxene rubber, cerium oxide reinforced particles, and a granule. In another exemplary embodiment, a method includes blending a liquid polyoxyxene rubber, cerium oxide enhancing particles, and abrasive particles to form a formulation. The method further includes forming a surface feature layer from the formulation and curing the formulation. In another exemplary embodiment, the abrasive article comprises a layer comprising a polyoxynoxy binder and abrasive particles. The layer has an elongation of at least about 50%. In another exemplary embodiment, the abrasive article comprises a surface feature layer configured to increase surface area with wear. The surface feature layer comprises a polyoxynoxy binder and abrasive particles. The surface feature layer has a thickness of no greater than about 500 mils. The abrasive article has no backing. In another exemplary embodiment, the abrasive article comprises a layer having surface protrusions. This layer includes a polysulfide oxygen spotting agent and a grinding philosopher. The abrasive article has a gloss performance of at least 122,813.doc 1337915 of about 20. In an additional embodiment, a method of conditioning a painted surface includes abrading a painted surface with an abrasive article formed from a cured formulation. The formulation includes liquid polyoxyxene rubber, cerium oxide reinforced particles, and abrasive particles. The method further includes polishing the ground painted surface. In another exemplary embodiment, a method of trimming a painted surface includes abrading a painted surface with an abrasive article, the abrasive article comprising a surface feature layer configured to increase in surface area with wear. This layer comprises a polyoxynoxy binder and abrasive particles. The abrasive article has no backing. The method further includes polishing the textured surface of the grind. [Embodiment]

在一特定實施例中,研磨物件係由形成表面特徵層之研 磨調配物形成。在-實施例中,$磨物件無背層(亦即無 結構背層)’因此物件係自行支撐。特定言之,形成表面 特徵層之調配物係自行支撐,以使得該層在研磨特性耗盡 之前耐用而無結構退化。在-實例中,調配物包括聚石夕氧 樹脂、微細增強顆粒及研磨粒。在一特定實例中,聚矽氧 樹脂係由液體聚矽氧橡膠形成,其通常包括如二氧化矽之 微細增強顆粒。表面特徵層包括表面突起之組合。表面突 起之組合可為隨機的且在一實施例中形成圖案。另外,橫 截面表面積可在物件磨損期間改變(通常 = 側壁傾斜之表面突起(棱錐、圓雜、棱柱等表面)突起= 况下,或可在磨損期間具有大體上恆 諸如在側壁垂直之突起(矩护、 、 、面積, 大起(矩形正方形、桿形等突起)之狀 1228I3.doc 1337915 況下。在一例示性實施例中,研磨物件亦可包括黏著層。 在另-例示性實施财,—卿成研磨物件之方法包括 心合液體聚梦氧橡膠及研磨粒以形成調配物。液體聚石夕氧 橡膠通常包括二氧化石夕增強顆粒。使用該調配物 特徵層,諸如包括如上所述之表面突起組合之表面特徵 層。另外,忒方法包括使調配物固化,形成表面特徵層。 或者,可使用熱塑性或其他熱固性聚合物形成研磨物件。 在一例示性實施例中,研磨物件包括由聚合物調配物及 研磨粒形成之表面特徵層。聚合物調配物可為熱塑性調配 物。或者,聚合物調配物可為可固化調配物。在另—實例 中,聚合物調配物可為可固化調配物與熱塑性調配物之組 合,諸如熱塑性硫化橡膠。在一特定實例中,熱塑性調配 物為熱塑性彈性體。在另一實例中,聚合物調配物可包括 具有不大於約25°C之玻璃轉移溫度之組份。舉例而言,聚 合物調配物可為多種聚合物之摻合物,其中聚合物之一具 有不大於約25°C之玻璃轉移溫度,或聚合物調配物可為嵌 段共聚物’其中嵌段組份之特徵為個別具有不大於約2 5 之玻璃轉移溫度之聚合物單元。詳言之,聚合物調配物可 包括不大於約10 wt%(諸如,不大於約5 wt%或甚至不大於 約3 wt%)之量的低玻璃轉移溫度組份。 例示性聚合物調配物包括聚醯胺-聚醚共聚物;聚酯-聚 _共聚物;丙烯酸樹脂、丙烯酸系共聚物,或經改質之丙 烯酸系共聚物’諸如乙烯-甲基丙烯酸酯共聚物、乙烯-曱 基丙烯酸酯-順丁烯二酸酐共聚物、聚甲基丙烯酸丁酯或 122813.doc 1Λ 1337915 甲基丙烯酸甲酯-甲基丙烯酸丁酯共聚物;乙烯_乙酸乙烯 酯共聚物;乙烯-乙酸乙烯酯-順丁烯二酸酐共聚物;二烯 彈性體;熱塑性聚胺基曱酸酯;聚乳酸與聚己内酯聚矽 氧烷共聚物之摻合物;聚矽氧樹脂;或其任何摻合物或任 何組合。例示性聚醯胺-聚醚可以商品名Pebax自Arkema購 得,諸如Pebax 2533。例示性丙烯酸系聚合物(包括共聚物 及經改貝之共聚物)可以商品名〇revac、Lotryi及L〇ta(Jer自 鲁 Arkema購得或以商品名EWac丨te自Lucke購得。例示性聚 酯-聚醚共聚物可以商品名Riteflex自Tic〇na購得。例示性 熱塑性聚胺基甲酸酯可以商品名Elast〇l丨an自BASF購得。 例不性二烯彈性體包括乙烯、丙烯及二烯單體之共聚物 (EPDM) 〇例不性二烯單體包括共軛二烯,諸如丁二烯、 異戊一烯、氣丁二烯或其類似物;包括5至約25個碳原子 之非共軛二烯’諸如丨,4_戊二烯、M-己二烯、l,5-己二 稀、2,5-二甲基-1,5-己二烯、M辛二稀或其類似物;環 φ 狀—烯,諸如%戊二烯、環己二烯、環辛二烯、二環戊二 烯或其類似物;乙烯基環烯,諸如丨乙烯基_丨_環戊烯、^ 乙烯基-i-環己烯或其類似物;烷基雙環壬二烯,諸如3_甲 基雙壞-(4,2,1)-壬-3,7-二烯或其類似物;茚,諸如曱基四 1節或其類似物;稀基降冰片稀,諸如5亞乙基_2降冰片 :»#、5-亞丁基-2-降冰片稀、2_曱代稀丙基5-降冰片烯、2_ 異丙烯基-5-降冰片烯、5 (a己二烯基降冰片烯、5_ (3,7辛—稀基)-2-降冰片烯或其類似物;三環二稀,諸如 3-曱基三環(5,2,1,。2,6)、癸二稀或其類似物丨或其任何 122S13.docIn a particular embodiment, the abrasive article is formed from a grinding formulation that forms a surface feature layer. In the embodiment, the article has no backing layer (i.e., an unstructured backing layer) so that the article is self-supporting. In particular, the formulation forming the surface feature layer is self-supporting such that the layer is durable without structural degradation before the abrasive properties are exhausted. In the examples, the formulations include polyoxin, fine reinforcing particles, and abrasive particles. In a specific example, the polyoxyxene resin is formed from a liquid polyoxyxene rubber, which typically includes fine reinforcing particles such as cerium oxide. The surface feature layer includes a combination of surface protrusions. The combination of surface protrusions can be random and form a pattern in one embodiment. In addition, the cross-sectional surface area may change during wear of the article (typically = surface protrusions of the sidewalls (pyramids, rounds, prisms, etc.) protrusions = or may be substantially constant during wear such as protrusions perpendicular to the sidewalls ( In the case of an exemplary embodiment, the abrasive article may also include an adhesive layer. In another example, the implementation of the invention may be carried out in the case of a large-scale (rectangular square, rod-shaped, etc.) 1228I3.doc 1337915. - The method of grinding an object comprises a heart-filled liquid polyoxymethylene rubber and abrasive particles to form a formulation. The liquid polyoxo rubber usually comprises a cerium oxide reinforced particle. The use of the formulation layer, such as The surface feature layer of the surface protrusion combination is described. In addition, the method comprises curing the formulation to form a surface feature layer. Alternatively, the abrasive article can be formed using a thermoplastic or other thermoset polymer. In an exemplary embodiment, the abrasive article comprises a surface feature layer formed from a polymer formulation and abrasive particles. The polymer formulation can be a thermoplastic formulation. The formulation may be a curable formulation. In another example, the polymer formulation may be a combination of a curable formulation and a thermoplastic formulation, such as a thermoplastic vulcanizate. In a particular example, the thermoplastic formulation is a thermoplastic elastomer. In another example, the polymer formulation can include a component having a glass transition temperature of no greater than about 25° C. For example, the polymer formulation can be a blend of a plurality of polymers, wherein the polymer A glass transition temperature having a temperature of no greater than about 25 ° C, or the polymer formulation can be a block copolymer wherein the block component is characterized by individual polymer units having a glass transition temperature of no greater than about 25. In other words, the polymer formulation can include a low glass transition temperature component in an amount of no greater than about 10 wt%, such as no greater than about 5 wt% or even no greater than about 3 wt%. Exemplary polymer formulations include Polyamine-polyether copolymer; polyester-poly-copolymer; acrylic resin, acrylic copolymer, or modified acrylic copolymer such as ethylene-methacrylate copolymer, ethylene-ruthenium Acrylate-maleic anhydride copolymer, polybutyl methacrylate or 122813.doc 1Λ 1337915 methyl methacrylate-butyl methacrylate copolymer; ethylene-vinyl acetate copolymer; ethylene-vinyl acetate Ester-maleic anhydride copolymer; diene elastomer; thermoplastic polyamino phthalate; blend of polylactic acid and polycaprolactone polyoxyalkylene copolymer; polyoxyl resin; or any blend thereof An exemplified polyamine-polyether is commercially available from Arkema under the trade name Pebax, such as Pebax 2533. Exemplary acrylic polymers (including copolymers and modified copolymers) can be traded under the trade name 〇revac , Lotryi and L〇ta (Jer purchased from Arkema or purchased from Lucke under the trade name EWac丨te. Exemplary polyester-polyether copolymers are commercially available from Tic〇na under the trade name Riteflex. Exemplary thermoplastic polyurethanes are commercially available from BASF under the tradename Elast®. Examples of non-diene elastomers include copolymers of ethylene, propylene and diene monomers (EPDM). Examples of non-diene monomers include conjugated dienes such as butadiene, isoprene, and gas butadiene. Or an analogue thereof; a non-conjugated diene comprising from 5 to about 25 carbon atoms such as anthracene, 4-pentadiene, M-hexadiene, 1,5-hexane dibasic, 2,5-dimethyl -1,5-hexadiene, M octane or the like; a ring-like olefin, such as % pentadiene, cyclohexadiene, cyclooctadiene, dicyclopentadiene or the like; Vinyl cyclic alkene, such as fluorenyl vinyl 丨 环 _ cyclopentene, vinyl-i-cyclohexene or the like; alkyl bicyclo decadiene, such as 3-methyl double bad - (4, 2, 1) - indole-3,7-diene or an analogue thereof; anthracene, such as a fluorenyl group 1 or an analog thereof; a thin base of borneol, such as 5 ethylene-2-norborn: »#, 5- Butylene-2-norborner, 2_deuterated propyl 5-norbornene, 2_isopropenyl-5-norbornene, 5 (a hexadienylnorbornene, 5_(3,7 xin) - dilute)-2-norbornene or an analogue thereof; tricyclic di-salt, such as 3-mercaptotricyclo (5,2,1,2,6), bismuth or Shu analogs, or any 122S13.doc

• 1U 1337915 組合。在-特定實施例中,二烯包括非共輕二稀。在另一 實施例中,二稀彈性體包括烯基降冰片稀。二稀彈性體可 包括(例如)以二烯彈性體之總重量計該聚合物之約63加% 至約95 wt〇/〇之乙稀、約5 wt%至約37 之丙稀及約〇 2 ㈣至約15 之二稀單體。在—料實例中,乙稀含量 為二稀彈性體之約70 wt%至約90 wt%,丙稀含量為二稀彈 性體之約心⑼至㈣—’且二稀單體含量為二稀彈性 體之約2 Wt%至約10 wt%。例示性二稀彈性體可以商品名 Norde!自 Dow賭得,諸如 Ν〇_ Ip 4725}>或-㈣ 482〇。 在一特定實施例中,聚合物調配物包括聚石夕氧樹脂。舉 例而言,聚石夕氧樹脂可由高黏度聚石夕氧橡膠(hcr)或液體 聚石夕氧橡膠(LSR)形成且可包括發煙二氧切增強填料。 在-特定實例中m樹脂係由LSR形成。—般而言, 聚石夕氧橡膠、LSR或HCR交聯形成聚石夕氧樹脂,其形成研 磨粒可分布或分散於其中之基質。該交聯聚石夕氧樹脂充當 研磨粒之點合劑且與組態成遷移至研磨物件表面之未交聯 聚矽氧形成對比。 聚夕氧樹月曰亦可由聚石夕氧油形成’通常所獲得之聚石夕氧 :由不含發煙二氧化矽。在此狀況下1聚矽氧油(部分A及 二、增強顆粒(諸如發煙二氧化修研磨粒 现後使其固化以形成聚矽氧樹脂。 :示性聚石夕氧油或聚石夕氧橡膠包括可連接官能基之石夕氧 ::主鏈。在—實例中’官能基可包括非反應性官能 基,堵如齒素基團、苯基或烧基或其任何組合。舉例: 122813.doc 之氟官能基。在另—例示 至甲基、乙基或丙基或其 可包括用以增強交聯之反 基包括氫陰離子基團、經 而言,矽氧烷聚合物可包 聚烷基矽氧烷或其任何組 應性§能基。在一特定實 氧烧及父聯劑形成。在— 。在一特定實例中,交聯 包括反應性氫陰離子官能 言’氟聚#氧可包括連接至主鍵 性實施例中’矽氧烷主鏈可連接 任何組合n錢烧主鏈亦 應性官能基。例示性反應性官能 基、乙烯基或其任何組合。舉例 括聚氟矽氧烷、聚苯基矽氧烷、 合,其具有諸如末端乙烯基之反 例中,聚石夕氧樹脂係由基物聚石夕 實例中,交聯劑可為有機交聯劑 劑為以聚矽氧為主之交聯劑,其 基0 表面特徵層可由未固化之調配物形成,該調配物可包括• 1U 1337915 combination. In a particular embodiment, the diene comprises a non-co-light dilute. In another embodiment, the dilute elastomer comprises an alkenyl norborner. The dilute elastomer may comprise, for example, from about 63% to about 95% 〇/〇 of the polymer, from about 5 wt% to about 37 propylene and about 〇 based on the total weight of the diene elastomer. 2 (d) to about 15 bis of dilute monomer. In the example of the material, the ethylene content is about 70 wt% to about 90 wt% of the dilute elastomer, and the propylene content is about the center of the dilute elastomer (9) to (4)-' and the dilute monomer content is dilute. The elastomer is from about 2 Wt% to about 10 wt%. Exemplary dilute elastomers can be traded under the trade name Norde! from Dow, such as Ν〇_Ip 4725}> or - (iv) 482〇. In a particular embodiment, the polymer formulation comprises polysorbate. For example, the polyoxo resin may be formed of a high viscosity polysulfide rubber (hcr) or a liquid polyoxo rubber (LSR) and may include a fumed dioxy-cut reinforcing filler. In a particular example the m resin is formed from an LSR. In general, polysulfide rubber, LSR or HCR crosslinks to form a polyoxin, which forms a matrix in which the abrasive particles can be distributed or dispersed. The crosslinked polyoxo resin acts as a point of abrasive particles and is in contrast to uncrosslinked polyoxymethylene configured to migrate to the surface of the abrasive article. The polyoxynium sulphate can also be formed from polysulfuric acid oil. The usually obtained polychlorite: from the absence of fuming cerium oxide. In this case, 1-polyoxygenated oil (parts A and II, reinforcing particles (such as fuming oxidized abrasive particles are now solidified to form a polyoxynoxy resin.: Illustrative polysulfuric acid or polylithic eve The oxy-rubber comprises a diarrhea::main chain to which a functional group may be attached. In the example, the 'functional group' may include a non-reactive functional group, such as a dentate group, a phenyl group or a burnt group, or any combination thereof. The fluoro functional group of 122813.doc is further exemplified to a methyl group, an ethyl group or a propyl group or a trans group which may be included to enhance crosslinking, and includes a hydrogen anion group. Polyalkyl siloxane or any group thereof § energy group. Formed in a specific oxy-fired and parent-linked agent. In a specific example, cross-linking includes reactive hydrogen anion functional words 'fluorine polymerization# Oxygen can include attachment to the primary bond embodiment. The 'oxyxane backbone can be attached to any combination of n-burning backbone functional groups. Exemplary reactive functional groups, vinyl groups, or any combination thereof. Examples include polyfluorinated fluorenes. Oxyalkane, polyphenyloxane, which has a counterexample such as a terminal vinyl group In the example of the polymetallic compound, the crosslinking agent may be an organic crosslinking agent, which is a polyfluorene-based crosslinking agent, and the base 0 surface characteristic layer may be formed by an uncured formulation. , the formulation may include

液體聚石夕氧橡膠(LSR)。舉例而t,#使用測試方法DIN 5: 〇19以10 s-i之剪切速率量測時,未固化之液體聚矽氧橡 膠可具有不大於600,000 cps之黏度。舉例而言,黏度可不 大於450,剛cps,諸如不大於cps。通t,黏度為 至少約50,000 cps,諸如至少約1〇〇,〇〇〇 cps。在另一實例 中,無增強顆粒之聚矽氧油之黏度可為約5 cps至約 165,000 cps ° 在固化調配物之狀況下,可將聚合物調配物在固化之前 與研磨粒且視情況與增強顆粒摻合。另外,可添加各種固 化劑、催化劑及熱引發劑或光引發劑及增感劑。在一例示 性實施例中,將聚矽氧橡膠與研磨粒摻合以提供調配物, Ik後使其固化。在一實例中,可使用過氧化物催化劑使調 122813.doc 1337915 配物固化。在另一實例中,可使用鉑催化劑使調配物固 化。在一特定實施例中,聚矽氧包括由鉑催化之兩部分液 體聚矽氧橡膠(LSR) »第一部分包括乙烯基末端或接枝之 聚烷基矽氧烷且第二部分包括交聯劑。在一特定實例中, 第一部分包括催化劑及抑制劑。在一額外實例中,交聯劑 可包括以矽氧烷為主之交聯劑,其具有連接反應性官能基 (諸如氫陰離子或羥基)之矽氧烷主鏈。 鲁 一般而言,將聚合物調配物在形成研磨物件之前與研磨 粒或增強顆粒摻合。當使用熱塑性聚合物調配物時,可將 研磨粒或增強顆粒與熔融狀態之聚合物調配物摻合。當裝 合物調配物為固化調配物時,可將研磨粒或增強顆粒與聚 合物e周配物之未固化組份摻合。因此,當冷卻或固化時, 聚合物調配物、研磨粒及可選之增強顆粒可形成複合材 料,其中研磨粒及可選之增強顆粒分布或分散遍布於聚合 物基質中。 ° • 在一例示性實施例中,將聚矽氧油與二氧化矽增強填料 及研磨粒摻合以形成調配物,隨後使其固化。在—實例 中’聚石夕氧油包括兩部分及始或過氧化物催化劑。第—部 分包括乙稀基末端或接枝之聚院基石夕氧烧且第二部分包括 交聯劑,諸如聚羥烷基矽氧烷。 由聚合物調配物形成之聚合物基質可展現理想 性,以使得由該聚合物調配物形成之研磨層可自' 從而能夠形成無背層物件。詳言之,該聚合物調配心用 乂 I成在研磨特性耗盡之前对用而無結構退化之研磨層。 I22813.doc 14 1337915 舉例而言,無研磨粒之¥ 之聚合物基質可展現理想斷裂伸長 率、拉伸強度或拉伸模數。與Λ丨二_ “ ㈣冑例而言,無研磨粒之聚合物 基貝可展現使用議53 5G4S1所測定之至少⑽%’諸如 至少約腑〇、至少約200%、至少約3〇〇%、至少約35〇%、 至少約450%或甚至至少約·%之斷裂伸長率。詳言之, 無研磨粒之具有二氧化石夕增強填料之聚石夕氧樹脂可具有使 用DIN 53 504 S1所測定之至少約35〇%,諸如至少約4鳩 或甚至至少約500%之斷裂伸長率。在另—實例中,無研 磨粒之固化聚石夕氧樹脂可具有至少約1〇 Mpa之拉伸強度。 在—例示性實_中,形成研磨物件之表面特徵層2調 配物可包括增強顆粒。舉例而言,可將增強顆粒併入聚矽 氧橡膠中。或者,可將增強顆粒在製備調配物的同時,諸 如在即將添加研磨粒之前添加至聚矽氧油中。例示性增強 顆粒包括二氧切顆粒、氧隸顆粒或其任何組合。 特定實例中,增強顆粒包括諸如發煙二氧化矽之二氧化 矽9例不性二氧化矽顆粒可以商品名Aerosil自Degussa購 得(諸如 Aerosil R812S)或自 Cab〇t c〇rp〇rati〇n 購得(諸如 sil 煙—氧化石夕)。在另一例示性實施例中,可將 增強二氧化矽併入液體聚矽氧橡膠調配物(諸如可自 Wacker SinCones購得之E】ast〇sil 3〇〇3調配物)中。—般而 。,增強顆粒分散在聚合物基質内且通常係單分散從而 大體上無聚結。 在另—例示性實施例中,經由基於溶液之方法形成之増 強顆粒(諸如溶膠形成及溶膠-凝膠形成之陶瓷)尤其適用於 122813.doc -15- 1337915 該調配物中。適合之溶膠可購得。舉例而言’水溶液中之 膠態二氧化石夕可以諸如”LUD〇x&quot;(E I Dup〇nt &amp; and Co., Inc. Wilmington, Del.) &gt; &quot;NYACOL'· (Nyacol Co.,Liquid polysulfide rubber (LSR). For example, t, # using test method DIN 5: 〇 19 When measured at a shear rate of 10 s-i, the uncured liquid polyoxyxene rubber may have a viscosity of no more than 600,000 cps. For example, the viscosity may be no greater than 450, just cps, such as no greater than cps. By t, the viscosity is at least about 50,000 cps, such as at least about 1 〇〇, 〇〇〇 cps. In another example, the non-reinforced particulate polyoxyxene oil may have a viscosity of from about 5 cps to about 165,000 cps °. In the case of a cured formulation, the polymer formulation can be cured prior to curing with the abrasive particles and optionally Enhanced particle blending. Further, various curing agents, catalysts, thermal initiators or photoinitiators and sensitizers may be added. In an exemplary embodiment, the polyoxyxene rubber is blended with the abrasive particles to provide a formulation which is then cured after Ik. In one example, a peroxide catalyst can be used to cure the modulating 122813.doc 1337915 formulation. In another example, the formulation can be cured using a platinum catalyst. In a particular embodiment, the polyoxyn oxide comprises a two-part liquid polyoxyethylene rubber (LSR) catalyzed by platinum. The first portion comprises a vinyl terminal or a grafted polyalkyl siloxane and the second portion comprises a crosslinking agent. . In a specific example, the first portion includes a catalyst and an inhibitor. In an additional example, the cross-linking agent can include a rhodium-based cross-linking agent having a decane backbone linked to a reactive functional group such as a hydride or a hydroxyl group. In general, the polymer formulation is blended with the abrasive particles or reinforcing particles prior to forming the abrasive article. When a thermoplastic polymer formulation is used, the abrasive particles or reinforcing particles can be blended with the molten polymer formulation. When the composition formulation is a cured formulation, the abrasive particles or reinforcing particles can be blended with the uncured component of the polymer e-weekly formulation. Thus, when cooled or cured, the polymer formulation, abrasive particles, and optional reinforcing particles can form a composite wherein the abrasive particles and optional reinforcing particles are distributed or dispersed throughout the polymeric matrix. ° • In an exemplary embodiment, the polyoxygenated oil is blended with the ceria reinforcing filler and abrasive particles to form a formulation which is subsequently cured. In the <RTIgt; </RTI> <RTIgt; </ RTI> <RTIgt; </ RTI> <RTIgt; The first portion includes a vinyl terminal or grafted polysulfide and the second portion includes a crosslinking agent such as a polyhydroxyalkyl siloxane. The polymer matrix formed from the polymer formulation can exhibit the desired properties such that the abrasive layer formed from the polymer formulation can be self-forming to form a backless article. In particular, the polymer blends the core with an abrasive layer that is used without structural degradation before the abrasive properties are exhausted. I22813.doc 14 1337915 For example, a polymer matrix without abrasive particles can exhibit an ideal elongation at break, tensile strength or tensile modulus. In the case of ( _ “ “ “ “ “ “ “ “ “ “ 聚合物 聚合物 聚合物 聚合物 聚合物 聚合物 聚合物 聚合物 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨 研磨An elongation at break of at least about 35%, at least about 450%, or even at least about %. In particular, the non-abrasive granules having a silica dioxide reinforcing filler may have a DIN 53 504 S1. The elongation at break is determined to be at least about 35%, such as at least about 4 or even at least about 500. In another example, the non-abrasive-cure polyclay may have a pull of at least about 1 MPa. In the exemplary embodiment, the surface feature layer 2 forming the abrasive article may comprise reinforcing particles. For example, the reinforcing particles may be incorporated into the polyoxyxene rubber. Alternatively, the reinforcing particles may be prepared. While the formulation is added to the polyoxyxide oil just prior to the addition of the abrasive particles. Exemplary reinforcing particles include dioxo particles, oxygen particles, or any combination thereof. In a particular example, the reinforcing particles include, for example, fumes.二 二 二 9 The erbium dioxide particles are commercially available from Degussa under the trade name Aerosil (such as Aerosil R812S) or from Cab 〇tc 〇rp〇rati〇n (such as sil smear - oxidized sulphur). In another exemplary embodiment The reinforced cerium oxide can be incorporated into a liquid polyoxyxene rubber formulation such as the E ast〇sil 3〇〇3 formulation available from Wacker SinCones. Typically, the reinforcing particles are dispersed in the polymer. Within the matrix and usually monodisperse to be substantially free of coalescence. In another exemplary embodiment, the labile particles formed by the solution based method, such as sol formation and sol-gel formed ceramics, are particularly suitable for use in 122813. Doc -15- 1337915. Suitable sols are commercially available. For example, 'colloidal silica in an aqueous solution can be such as "LUD〇x&quot; (EI Dup〇nt &amp; and Co., Inc. Wilmington, Del.) &gt;&quot;NYACOL'· (Nyacol Co.,

As.nd,Ma,)或&quot;NALc〇,,(Nale。心心31 c。,⑽―呔 I丨1.)之商品名購得。許多市售溶膠為鹼性的可由鹼金 屬’諸如氫氧化納、氫氧化卸或氫氧化敍來穩定。適合之 膠態二氧化矽之額外實例係描述於美國專利第5,126,394號 中,其以引用方式併入本文中。尤其適合者為溶膠形成之 二氧化矽及溶膠形成之氧化鋁。可藉由使一或多種適合之 表面處理劑與溶膠中之無機氧化物基質粒子反應來使溶膠 官能化。 在一特定實施例中,增強顆粒具有亞微米大小。增強顆 粒可具有在約50 m2/g至約500 ^/§之範圍内,諸如在約 1 0, m /g至,’勺400 m /g之範圍内之表面積。增強顆粒可為 奈米大小之顆粒,諸如具有約3 nm至約5〇〇 nm之平均粒度 之顆粒。在一例示性實施例中,增強顆粒具有約3⑽至約 2〇〇nm,諸如約3nm至約1〇〇nm、約3nm至約5〇邮、約8 nm至約30 nm或約nm至約25 nm之平均粒度。在特定實 施例中,平均粒度不大於約5〇〇_,諸如不a_2qq⑽ 或不大於約15〇 nm。對於增強顆粒,平均粒度可定義為對 應於小角度中子散射(讀5)分布曲線中之峰值體積分數的 粒度或對應於SANS分布曲線之0.5累積體積分數之粒度。 增強顆粒亦可由#有不大於平均粒度約2 〇倍之半又寬的 狹窄分布曲線表徵。舉例而言’半寬可不大於約^或不 I22813.doc 16 15 :约1·〇。分布之半寬為最大高度一半(諸如分布曲線峰 Α處之粒子分數的—半)處之分布曲線之寬度。在一特定 &amp;例令’粒度分布曲線為單峰式的。在—替代實施例 中,粒度分布為雙峰式的或在粒度分布中具有一個以上峰 值。 έ:一:例中’增強顆粒以聚矽氧、增強顆粒及研磨粒之 組合重里計以-定量包括於調配物中。舉例而言,增強顆 ^包括增強顆粒、聚梦氧樹脂及研磨粒之調配物之總重 1。十可以至少約3 wt%之量包括於調配物中。詳言之,調 配物可包括至少約5 ·增強顆粒,諸如至少約10 wt% 曰強顆粒’或甚至至少約j 3 wt%之增強顆粒。另外,調 配物可包括不大於約6〇 wt%之增強顆粒,諸如不大於約% wt%之增強顆粒。 調配物可進—步包括研磨粒。研磨粒可由包括以下各物 之研磨粒中之任—者或其組合形成:二氧化%、氧化紹 (炫融或燒結)、氧化錯、氧化錯/氧化紹、碳化石夕、石權 石' 金剛石、立方氮化硼、氮切、二氧㈣、二氧化 鈦、二棚化鈦、碳化硼、氧化錫、碳化鎢、碳化欽、氧化 鐵、氧化鉻、燧石、金剛砂或其任何組合。舉例而言,研 磨粒可選自由以下各物組成之群:二氧化石夕、氧化紹、氧 化錯、碳化石夕、氮化石夕、氮化蝴、石梅石、金剛石、址炫 氧化叙氧化錯、二氧化鋪、二删化欽、碳化删、熥石、金 :砂=紹或其推合物。詳言之,研磨粒可選自由氮化 、氧化物、碳化物或其任何組合組成之群。在一實例 J22813.doc 1337915 中,氮化物可選自由立方氮化硼 成&lt; #。4 s „ 氮化矽或其任何組合組 f在另一貫例中,氧化物 群:_I j、自由以下各物組成之 一氧化矽、氧化鋁、氧化錯、 JL· t±: 氣化t /氧化紹、二氧 ,申、一氧化鈦、氧化錫、氧化鐵、 入。y- — 乳化路或其任何組 σ 在另一貫例中,碳化物可選έ i。 化μ 物八自由碳化砂、碳化硼、碳 化鎢、奴化鈦或其任何組合組 . 砂。— 珉之群,且尤其可包括碳化 夕特疋貫施例使用主要包含α•氣仆如 氧化紹之緻密研磨粒。在 • 另一特疋貫例中,研磨粒包括碳化矽。 研磨粒亦可具有特定形狀。該 _ . 〜狀之一貫例包括桿形、 二角形、稜錐、圓錐、實心球' 工“球或其類似形狀。或 - 者,研磨粒可具有任意形狀。 研磨粒通常具有不大於2〇〇〇微半,4上 微水诸如不大於約1500微As.nd, Ma,) or &quot;NALc〇,, (Nale. Heart 31 c., (10) - 呔 I丨1.) The trade name is purchased. Many commercially available sols are basic and can be stabilized by an alkali metal such as sodium hydroxide, hydroxide or hydrogen hydroxide. An additional example of a suitable colloidal cerium oxide is described in U.S. Patent No. 5,126,394, incorporated herein by reference. Particularly suitable are cerium oxide formed by sol and alumina formed by sol. The sol can be functionalized by reacting one or more suitable surface treatment agents with the inorganic oxide matrix particles in the sol. In a particular embodiment, the reinforcing particles have a submicron size. The reinforcing particles may have a surface area in the range of from about 50 m2/g to about 500^/§, such as in the range of from about 10, m / g to , 'spoon 400 m / g. The reinforcing particles may be nanometer sized particles such as particles having an average particle size of from about 3 nm to about 5 Å. In an exemplary embodiment, the reinforcing particles have from about 3 (10) to about 2 Å, such as from about 3 nm to about 1 〇〇 nm, from about 3 nm to about 5 Å, from about 8 nm to about 30 nm, or from about nm to about Average particle size of 25 nm. In a particular embodiment, the average particle size is no greater than about 5 Å, such as not a_2qq (10) or no greater than about 15 〇 nm. For reinforcing particles, the average particle size can be defined as the particle size corresponding to the peak volume fraction in the small angle neutron scattering (read 5) distribution curve or the particle size corresponding to the cumulative volume fraction of 0.5 of the SANS distribution curve. The reinforcing particles can also be characterized by a narrow distribution curve which is not more than half the average particle size of about 2 〇. For example, the half width may be no more than about ^ or not I22813.doc 16 15 : about 1 〇. The half width of the distribution is the width of the distribution curve at half the maximum height (such as the half of the particle fraction at the peak of the distribution curve). In a particular &amp; order, the particle size distribution curve is unimodal. In an alternative embodiment, the particle size distribution is bimodal or has more than one peak in the particle size distribution. έ: One: In the example, the reinforcing particles are included in the formulation by a combination of polyoxymethylene, reinforcing particles and abrasive particles. For example, the reinforcing particles include the total weight of the formulation of the reinforcing particles, the polyoxyl resin, and the abrasive particles. Ten may be included in the formulation in an amount of at least about 3 wt%. In particular, the formulation may comprise at least about 5 - reinforcing particles, such as at least about 10% by weight of the sturdy particles' or even at least about 3% by weight of reinforcing particles. Additionally, the formulation may include no more than about 6% by weight of reinforcing particles, such as no more than about % by weight of reinforcing particles. The formulation can include, in addition, abrasive particles. The abrasive particles may be formed of any one or a combination of the abrasive particles including the following: % oxidation, oxidation (smelting or sintering), oxidation, oxidation, oxidation, carbonization, stone weight Diamond, cubic boron nitride, nitrogen cut, dioxane (tetra), titanium dioxide, titanium dioxide, boron carbide, tin oxide, tungsten carbide, carbon carbide, iron oxide, chromium oxide, vermiculite, silicon carbide or any combination thereof. For example, the abrasive particles can be selected from the group consisting of: sulphur dioxide, oxidized, oxidized, carbonized stone, nitriding, nitriding, stone, diamond, diamond, oxidation Wrong, dioxide oxidized, two sputum, carbonized, chert, gold: sand = Shao or its compound. In particular, the abrasive particles may be selected from the group consisting of nitrides, oxides, carbides, or any combination thereof. In an example J22813.doc 1337915, the nitride may be selected from cubic boron nitride to &lt;#. 4 s „ Tantalum nitride or any combination thereof f In another example, the oxide group: _I j, one of the following components: ruthenium oxide, aluminum oxide, oxidization error, JL·t±: gasification t / Oxidation, dioxane, sulphur, titanium oxide, tin oxide, iron oxide, in. y - emulsified road or any group of σ In another example, the carbide is optional έ i. , boron carbide, tungsten carbide, annihilated titanium or any combination thereof. Sand. - Groups of strontium, and especially carbonized sinter applications. The use of dense abrasive particles mainly containing α• gas servant such as oxidized. In another special case, the abrasive particles include tantalum carbide. The abrasive particles may also have a specific shape. The consistent example of the shape includes a rod shape, a quadrangular shape, a pyramid, a cone, a solid ball 'work' ball or Similar shape. Or - the abrasive particles can have any shape. The abrasive particles usually have a micro-half of not more than 2 inches, and 4 micro-waters such as no more than about 1500 micrometers.

米之平均粒經D為g Φ- U\ rU 伞) 在另一貫例中,研磨粒粒徑不大於750微 …4如不大於約350微米。舉例而言,研磨粒粒徑可為 至少〇.1微#,諸如約〇·】微米至約15〇〇微米,且更通常為 •約微米至約200微米或約1微米至約⑽微米。研磨粒之 粒徑通常規定為研磨粒之最長尺寸。一般存在一定範圍之 叔分布。在一些情形中’粒徑分布受到嚴格控制。 在一例示性調配物中,研磨粒占調配物重量之約10%至 約90%’諸如約30%至約8〇%。在一例示性實施例中調 配物包括以調配物之總重量計至少約%心之研磨粒。舉 例而吕,調配物可包括至少約45 wt%之研磨粒,諸如至少 約55·研磨粒。一般而言,調配物包括不大於%禮。 之研磨粒,諸如不大於85 wt%之研磨粒。 1228l3.doc ,又而έ,由包括聚合物調配物、研磨粒及可選之增強 顆粒之調配物形成表面特徵層。形成為層後調配物即展現 有利地增強由該調配物所形成之研磨物件之效能的機械特 性。詳言之,調配物可展現理想機械特性,諸如斷裂伸長 率、硬度、拉伸模數或板伸強度。另外,可評估研磨物件 在產生經研磨產品中所需之表面特性方面之效能。 在一例示性實施例中,調配物展現(例如)使用測試方法 ASTMD 412或測試方法DIN 53 504 S1所量測之至少約5〇% 之斷裂伸長率。詳言之,斷裂伸長率可為至少約1 〇〇% ’ 諸如至少約】2 5 %或甚至至少約1 3 5 % 〇 固化調配物亦可具有理想硬度,諸如基於測試方法 DIN53 505之在約50肖氏Α至約75肖氏D範圍内之硬度。舉 例而言,硬度可不大於約75肖氏D,諸如不大於6〇肖氏d 或不大於50肖氏D。 在另一例不性實施例中,調配物展現基於ASTM D 4】2 之在loo%應變下不大於約8 〇 MPa之理想拉伸模數。舉例 而言,拉伸模數可不大於約7·6 MPa,諸如不大於約7 5 MPa。另外,固化調配物可具有基於ASTMD4l22至少約 7.0 MPa之理想拉伸強度。舉例而言,固化調配物可具有 至少約7.5 MPa,諸如至少約8.〇 MPa之拉伸強度。或者, 调配物可展現至少約8 MPa,諸如至少約14 MPa或甚至至 少約30 MPa之拉伸模數。特定調配物可展現大於i〇〇 MPa 之拉伸模數。 调配物之機械特性可有助於研磨物件之效能諸如有利 122813.doc 1337915 地促進可由自該調配物形成之研磨物 叶運成之表面特性。 “列而言’固化調配物之機械特性可有助於表面效能特 性’諸如下文所定義之光澤效能或粗輪度效能。另外:研 磨物件可展現如由下文定義之移除4 由广乂疋我二移除札數表徵之理想材料移 除速率。The average grain diameter of rice is g Φ- U\ rU umbrella. In another example, the particle size of the abrasive grains is not more than 750 μm 4 , such as not more than about 350 μm. For example, the abrasive particles may have a particle size of at least 0.1 micrometers, such as from about 1 micrometer to about 15 micrometers, and more typically from about micrometers to about 200 micrometers or from about 1 micrometer to about (10) micrometers. The particle size of the abrasive particles is usually specified as the longest dimension of the abrasive particles. There is generally a range of uncle distributions. In some cases the particle size distribution is strictly controlled. In one exemplary formulation, the abrasive particles comprise from about 10% to about 90% by weight of the formulation, such as from about 30% to about 8%. In an exemplary embodiment, the formulation comprises at least about 5% of the abrasive particles of the total weight of the formulation. By way of example, the formulation may include at least about 45 wt% abrasive particles, such as at least about 55. abrasive particles. In general, the formulation includes no more than % ritual. The abrasive particles, such as abrasive grains of no more than 85 wt%. 1228l3.doc, in turn, forms a surface feature layer from a formulation comprising a polymer formulation, abrasive particles, and optionally reinforcing particles. Forming the post-layer formulation exhibits mechanical properties that advantageously enhance the effectiveness of the abrasive article formed by the formulation. In particular, the formulation exhibits desirable mechanical properties such as elongation at break, hardness, tensile modulus or panel strength. In addition, the effectiveness of the abrasive article in producing the desired surface characteristics in the milled product can be evaluated. In an exemplary embodiment, the formulation exhibits, for example, an elongation at break of at least about 5% as measured using test method ASTMD 412 or test method DIN 53 504 S1. In particular, the elongation at break may be at least about 1%%, such as at least about 25%, or even at least about 135%. The curing formulation may also have a desired hardness, such as based on test method DIN 53 505. 50 Shore Α to a hardness in the range of about 75 Shore D. For example, the hardness may be no greater than about 75 Shore D, such as no greater than 6 〇 Shore d or no greater than 50 Shore D. In another non-limiting embodiment, the formulation exhibits an ideal tensile modulus of no greater than about 8 MPa at loo% strain based on ASTM D 4]2. For example, the tensile modulus can be no greater than about 7.6 MPa, such as no greater than about 75 MPa. Additionally, the cure formulation can have an ideal tensile strength of at least about 7.0 MPa based on ASTM D4112. For example, the cure formulation can have a tensile strength of at least about 7.5 MPa, such as at least about 8. MPa. Alternatively, the formulation may exhibit a tensile modulus of at least about 8 MPa, such as at least about 14 MPa or even at least about 30 MPa. Specific formulations can exhibit tensile modulus greater than i 〇〇 MPa. The mechanical properties of the formulation can aid in the effectiveness of the abrasive article, such as the benefit 122813.doc 1337915, to promote surface properties that can be imparted by the abrasive particles formed from the formulation. "In terms of column, the mechanical properties of the curing formulation can contribute to surface performance characteristics such as gloss performance or coarse roundness performance as defined below. Additionally: the abrasive article can exhibit removal as defined below by 4 I removed the ideal material removal rate for the number of measurements.

在-例示性實施例中,該調配物可形成研磨物件之表面 特徵層。圖1包括例示性結構化研磨物件1〇〇之說明。或 H調配物可用於形成其他非結構化經塗佈研磨物件或 黏合研磨物件。通常,結構化經塗佈研磨物件包括具有通 常排列成圖案之突出表面結構之組合的經塗佈研磨物件。In an exemplary embodiment, the formulation can form a surface feature layer of the abrasive article. Figure 1 includes an illustration of an exemplary structured abrasive article. Or the H formulation can be used to form other unstructured coated abrasive articles or bonded abrasive articles. Typically, the structured coated abrasive article comprises a coated abrasive article having a combination of protruding surface features that are generally arranged in a pattern.

亦稱為工程研磨物件之結構化研磨物件含有複數個研磨 粒,其分散在黏合劑中且在研磨物件上或遍布其中以圖案 或隨機排列之形式形成離散的三維單元。結構研磨物件通 常具有相對較高之材料移除速率以及精細表面修整及較長 使用壽命。此等物件經設計《可磨#,從而連續地使新的 研磨劑暴露於研磨界面。然而,大多數結構化研磨物件係 為強力應用而設計。因此,當用於弱力應用中時,樹脂黏 合劑不會損耗或磨損以暴露新的研磨粒。 圖1中所說明之例示性結構化研磨物件丨〇〇包括研磨層 102。研磨層102包括可排列成囷案之突出結構1〇8。在所 说明之實施例中,突出結構1 〇8經組態成回應於磨損提供 增加之接觸面積,如在突起具有傾斜側表面之狀況下。舉 例而a,結構1 08可具有隨著與研磨層i 〇2底部之距離增加 而減小的橫戴面。通常,研磨層1〇2係由包括聚合物調配 I22813.doc -20. 1337915 物、增強顆粒及研磨粒之調配物形成。舉例而言,可使調 配物形成為圖案化層且固化或硬化以產生具有結構1 〇8之 研磨層.1 0 2。 在一例示性實施例中,可形成具有背層或支撐層之研磨 層102。背層通常係直接黏合至研磨層1〇2且直接接觸研磨 層102。舉例而言,可將研磨層102擠壓至或壓延至背層 上。背層或支撐層可包括聚合物薄膜、聚合物發泡體或纖 維織物。在一特定實例中,背層或支撐層可包括布、紙或 ΊΊ ...a 6 通吊’背層或支推層為不包括研磨粒之非研 磨層。背層或支撐層—般提供結構性支撐或賦予研磨物件 可提高研磨層102效能之機械特性。 或者,研磨物件100可無背層,用於形成研磨層1〇2之特 定調配物提供理想機械特性且可自行支樓。亦即,研磨層 102可經組態成在使用中或在製造期間不依賴於背層。舉 例而吕,自行支撑之研磨層102可在研磨特性耗盡之前耐 用而無結構退化。詳言之,調配物中之聚合物之特性可允 ,形成無背層研磨物件100 ’其可具有優於一般需要使用 背層以在1個塗佈過程中承載研磨層且在使用期間提供機 械完整性或可撓性的目前技術水平之特定優點。詳言:, 在無下伏支樓層或背層存在之情況下’研磨層102可自行 支撐。5亥等下伏支撐層或背層傳統上具有優於傳統研磨声 ::伸特性(強度與可撓性之組合)。在此特定實施例t: 層。物件100不含拉伸特性優於研磨層102之拉伸特性之 122813.doc 1337915 除研磨層102外’研磨物件1〇〇可包括黏著層】〇4。舉例 而言,黏著層Π)4可包括愿敏性黏接劑或固化點接劑。當 使㈣接劑將研磨物件與研磨工具黏合時,可用隔離薄膜 覆蓋研磨層以防止提前黏著。該等隔離薄膜通常係在即將 使研磨物件Η)0連接至研磨工具之前移除。在圖7中所說明 之一特定實施例中,黏著層7〇4可形成下表面,諸如麼敏 性黏接表面,且具有表面特徵7〇8之研磨層7〇2可形成研磨 性上表面。詳言之,黏著層7〇4係與研磨層7〇2直接接觸而 (諸如)無插入結構層。 在另一例示性實施例中’黏著層1〇4可黏合至扣件板 ]〇6。詳言之,扣件板1〇6可用以將研磨產品耦接至研磨 機。在一實例中,扣件板1〇6並非經組態成向研磨物件提 供結構性支撐。舉例而言,扣件板i 〇6可具有小於研磨層 102之拉伸強度》在_實例中,扣件板1 〇6可為卡鉤及環圈 固定系統之一組件。該固定系統可用於將研磨物件1〇〇耦 接至研磨工具。 研磨物件100之結構108可排列成圖案。舉例而言,圖2 及圖3包括研磨結構之例示性圖案之說明。在一例示性實 施例中’圖2說明併入至研磨層202中之研磨結構2〇4之圖 案200。舉例而言,研磨結構204排列成柵格圖案。在另一 例示性實施例中’圖3包括圖案3〇〇之說明,其中稜柱形研 磨結構304併入至研磨層3〇2中。如所說明,稜柱形結構 3 04排列成平行線。或者,該等結構可無確定圖案地隨機 排列’或元件可在交替列或行中彼此偏移。在一額外實例 122813.doc • 11· 1337915 中,結構108可為具有傾斜側壁之離散突起。在另—實例 中,結構108可為具有大體上垂直之侧壁之離散突起。結 構1 08可排列成具有圖案之陣列或可排列成隨機陣列。 在-實施例中,突出於研磨層之研磨結構經組態成回應 於磨損增加接觸面積。舉例而言,圖4及圖5包括研磨結構 之例示性橫截面之說明。圖4包括具有三角形橫裁面之研 磨結構400。在第一磨損程度之狀況下,由寬度4〇2所指示 之接觸面積小於由額外磨損所得之接觸面積,諸如接觸面 積404。大體上形成於408所指示之水平面中之接觸面積通 常隨406所指示之垂直高度降低而增加。在另一例示性實 施例中,結構可具有半圓形橫截面500,其中接觸表面5〇4 大於由較少磨損所得之接觸表面,諸如表面5〇2。雖然圖4 及圖5中所說明之垂直橫裁面為規則形狀,但結構或突起 可具有不規則形狀或規則形狀。若具有規則形狀,則突起 可具有水平橫截面,諸如圓形或多邊形。 回到圖1 ’已發現上述調配物尤其適用於形成特定結構 化研磨物件,尤其是不具支撐層或背層且包括薄結構之研 磨物件。在一例示性實施例中,研磨層】〇2具有以字母B表 示之總高度,其不大於約500密耳,諸如不大於約35〇密 耳,不大於約200密耳,不大於約1〇〇密耳,不大於約5〇密 耳或甚至不大於約35密耳。研磨結構1〇8可不大於約2〇密 耳’諸如不大於約15密耳。另外,以字母C表示的不包括 研磨結構1〇8之研磨層1〇2之寬度可不大於約15密耳,諸如 不大於約1 〇密耳。 122813.doc -23- 1337915 在一例示性實施例中,研磨物件可使用如圖6中所說明 ,方法_來形成。舉例而言’如6〇2所說明,可將聚:夕氧 Λ研磨粒混合。在-特定實施例巾,將包括二氧化矽辦強 顆粒之液體聚⑦氧㈣與研磨粒混合以形成未固化调配 =。另夕卜,混合可包括混合液體聚石夕I橡膠之部分Α與部 刀Β。或纟’混合可包括以各種順序之一混合聚矽氧油、 增強顆粒及研磨粒以形成調配物。A structured abrasive article, also known as an engineered abrasive article, contains a plurality of abrasive particles dispersed in a binder and forming discrete three-dimensional elements in or on the abrasive article in a pattern or random arrangement. Structural abrasive articles typically have a relatively high material removal rate as well as fine surface finish and long service life. These items are designed to be Grindable # to continuously expose the new abrasive to the grinding interface. However, most structured abrasive articles are designed for strong applications. Therefore, when used in a weak force application, the resin binder is not worn out or worn to expose new abrasive particles. The exemplary structured abrasive article 说明 illustrated in FIG. 1 includes an abrasive layer 102. The abrasive layer 102 includes a protruding structure 1〇8 that can be arranged in a file. In the illustrated embodiment, the protruding structure 1 〇 8 is configured to provide increased contact area in response to wear, such as where the protrusion has a sloping side surface. By way of example, a, structure 108 may have a cross-face that decreases as the distance from the bottom of polishing layer i 〇 2 increases. Typically, the abrasive layer 1〇2 is formed from a formulation comprising a polymer formulation I22813.doc -20. 1337915, reinforcing particles and abrasive particles. For example, the formulation can be formed into a patterned layer and cured or hardened to produce an abrasive layer having a structure of 1 〇8. In an exemplary embodiment, an abrasive layer 102 having a backing layer or a support layer can be formed. The backing layer is typically bonded directly to the abrasive layer 1〇2 and directly in contact with the abrasive layer 102. For example, the abrasive layer 102 can be extruded or calendered onto the backing layer. The backing layer or support layer may comprise a polymeric film, a polymeric foam or a fibrous web. In a particular example, the backing layer or support layer can comprise a cloth, paper or ’ a 6 hanged back layer or a push layer is a non-abrasive layer that does not include abrasive particles. The backing or support layer generally provides structural support or imparts mechanical properties to the abrasive article that enhance the effectiveness of the abrasive layer 102. Alternatively, the abrasive article 100 can be unbacked, and the particular formulation used to form the abrasive layer 1〇2 provides desirable mechanical properties and can be self-supporting. That is, the abrasive layer 102 can be configured to be independent of the backing layer during use or during manufacture. For example, the self-supporting abrasive layer 102 can be used without structural degradation before the abrasive properties are exhausted. In particular, the properties of the polymer in the formulation allow for the formation of a backless abrasive article 100' which may have advantages over the general need to use a backing layer to carry the abrasive layer during one coating process and provide machinery during use. The specific advantages of the current state of the art for integrity or flexibility. In particular, the abrasive layer 102 can be self-supporting without the presence of an underlying floor or backing layer. The underlying support layer or back layer of 5 hai has traditionally been superior to the conventional grinding sound: stretching characteristics (combination of strength and flexibility). In this particular embodiment t: layer. The article 100 does not contain tensile properties superior to the tensile properties of the abrasive layer 102. 122813.doc 1337915 In addition to the abrasive layer 102, the abrasive article 1 can include an adhesive layer. For example, the adhesive layer 4 can include a positively sensitive adhesive or a curing point. When the (4) adhesive is used to bond the abrasive article to the abrasive tool, the abrasive layer may be covered with a barrier film to prevent adhesion in advance. The barrier films are typically removed just prior to attachment of the abrasive article Η)0 to the abrasive tool. In a particular embodiment illustrated in Figure 7, the adhesive layer 7A can form a lower surface, such as a viscous bonding surface, and the abrasive layer 7 〇 2 having surface features 7 可 8 can form an abrasive upper surface. . In particular, the adhesive layer 7〇4 is in direct contact with the abrasive layer 7〇2, such as without an intervening structural layer. In another exemplary embodiment, the adhesive layer 1〇4 can be bonded to the fastener plate 〇6. In particular, the fastener plates 1〇6 can be used to couple the abrasive product to the grinder. In one example, the fastener plates 1〇6 are not configured to provide structural support to the abrasive article. For example, the fastener panel i 〇 6 can have a tensile strength less than that of the abrasive layer 102. In the example, the fastener panel 1 〇 6 can be one of the components of the hook and loop fastening system. The fastening system can be used to couple the abrasive article 1〇〇 to the abrasive tool. The structures 108 of the abrasive article 100 can be arranged in a pattern. For example, Figures 2 and 3 include illustrations of exemplary patterns of abrasive structures. In an exemplary embodiment, FIG. 2 illustrates a pattern 200 of abrasive structures 2〇4 incorporated into the polishing layer 202. For example, the abrasive structures 204 are arranged in a grid pattern. In another exemplary embodiment, 'Fig. 3' includes an illustration of a pattern 3〇〇 in which a prismatic abrasive structure 304 is incorporated into the abrasive layer 3〇2. As illustrated, the prismatic structures 306 are arranged in parallel lines. Alternatively, the structures may be randomly arranged without a defined pattern&apos; or the elements may be offset from one another in alternating columns or rows. In an additional example 122813.doc • 11· 1337915, the structure 108 can be a discrete protrusion having sloping sidewalls. In another example, structure 108 can be a discrete protrusion having substantially vertical sidewalls. The structures 108 may be arranged in an array having a pattern or may be arranged in a random array. In an embodiment, the abrasive structure protruding from the abrasive layer is configured to increase the contact area in response to wear. For example, Figures 4 and 5 include illustrations of exemplary cross sections of the abrasive structure. Figure 4 includes a grinding structure 400 having a triangular cross-section. In the case of the first degree of wear, the contact area indicated by the width 4 〇 2 is smaller than the contact area obtained by the additional wear, such as the contact area 404. The contact area generally formed in the horizontal plane indicated by 408 generally increases as the vertical height indicated by 406 decreases. In another exemplary embodiment, the structure can have a semi-circular cross-section 500, wherein the contact surface 5〇4 is larger than the contact surface resulting from less wear, such as surface 5〇2. Although the vertical cross-sections illustrated in Figures 4 and 5 are of a regular shape, the structure or protrusion may have an irregular shape or a regular shape. If it has a regular shape, the protrusions may have a horizontal cross section such as a circle or a polygon. Returning to Figure 1 'the above formulation has been found to be particularly useful for forming a particular structured abrasive article, particularly a abrasive article that does not have a support or backing layer and that includes a thin structure. In an exemplary embodiment, the abrasive layer 〇 2 has a total height indicated by the letter B, which is no greater than about 500 mils, such as no greater than about 35 mils, no greater than about 200 mils, and no greater than about 1 〇〇 mil, no more than about 5 mils or even no more than about 35 mils. The abrasive structure 1 8 may be no greater than about 2 mils, such as no greater than about 15 mils. Additionally, the width of the abrasive layer 1〇2, represented by the letter C, excluding the abrasive structure 1〇8, may be no greater than about 15 mils, such as no greater than about 1 mil. 122813.doc -23- 1337915 In an exemplary embodiment, the abrasive article can be formed using a method as illustrated in FIG. For example, as illustrated by 6〇2, the poly-oxo-arsenic abrasive particles may be mixed. In a particular embodiment, a liquid polyoxygen (IV) comprising cerium oxide particles is mixed with the abrasive particles to form an uncured formulation =. In addition, the mixing may include mixing a portion of the liquid poly-stone I and the knives. Alternatively, mixing may include mixing the polyoxygenated oil, reinforcing particles, and abrasive particles in one of a variety of sequences to form a formulation.

如604所說明,可使用該調配物形成圖案化層。舉例而 言,圖案化層可包括經組態成回應於磨損提供增加之接觸 面積之表面結構圖案。舉例而言,可將固化調配物擠壓或 壓延成板。可對該板進行沖印、雕刻或整體圖案化或此等 方法之任何組合以提供圖案化表面結構。在另一例示性實 施例中’可將調配物擠壓或壓延至包括負片圖案之負片表 面(其中賦予負片表面用以形成圖案化層之圖案)上。 如606所說明,在由未固化調配物形成圖案化層後,即 可使調配物固化。在鉑催化之聚矽氧之狀況下,可將調配 物及由其形成之圖案化層加熱且因此使其熱固化。在替代 實施例中’可使用對光化輻射作出反應之催化劑系統。固 化之典型條件為在350°F下歷時5分鐘。 可使用熱塑性聚合物調配物實施類似方法。舉例而言, 可將熱塑性聚合物調配物與研磨粒及可選之增強顆粒摻 合。該摻合可在擠壓機或加熱摻合機中進行。可擠壓包括 聚合物調配物、研磨粒及增強顆粒之摻合調配物並使其圖 案化。舉例而言,可使用沖印、滾壓或其他圖案化技術在 1228l3.doc -24- 1337915 摻合調配物之擠壓層之表面中形成表面圖案。在特定實例 中’可將摻合調配物擠壓至負圖案化模具上。摻合調配物 可冷卻而形成研磨層。可添加黏著層或扣件層以形成研磨 產品。或者,可對此方法進行修改以用於熱塑性硫化橡 膠。 雖然研磨物件之實施例可用於各種工業應用中,但研磨 物件之特定實施例係有利用於諸如光學媒體修復業之表面 _ 處理業中。舉例而言,可使用預打磨處理對諸如光學媒體 或塗漆表面之經處理表面進行研磨。預打磨通常係使用粗 粒研磨物件來進行且通常移除大的表面缺陷而留下亞光毛 - 面。在一例示性實施例中,使用具有小於粗粒研磨物件之 • 粒徑的研磨物件進一步研磨經預打磨之表面。舉例而言, 可使用由上述調配物形成之研磨物件進一步研磨經預打磨 之表面。該調配物可包括聚合物調配物、二氧化♦增強顆 粒及研磨粒。 • 在另一實例中,可使用包括具有經組態成表面積隨著磨 損而增加之表面圖案之層的研磨物件進一步研磨經預打磨 之表面。該層可包括聚合物調配物及研磨粒。研磨物件可 無背層。 在研磨之後,可磨光或拋光經研磨之表面。舉例而古, 可用羊毛塾或發泡體墊磨光或拋光經研磨之表面。經磨光 或拋光之表面通常具有理想粗糙度及光澤。 在一特定實施例中,研磨物件可用於修復諸如cd或 DVD之光學媒體。舉例而言,CD或DVD租賃機構或轉售 122813.doc -25- 1337915 者可接收用舊的光學媒體。在一實例中,機構可經由店鋪 接收光學媒體。在另_實例中,機構可經由郵寄接收光學 媒體。可用如上所述形成之研磨物件研磨或DVC)。在 特疋實例中,研磨物件不包括背層。在另一實例中,研磨 物件可包括壓敏性黏接表面。可清潔及拋光或dVD。 iW後,可提供CD或DVD用於後續使用,諸如再次租賃或 銷。3羊5之,該等研磨物件適用於不使用後續塗佈過程The formulation can be used to form a patterned layer as illustrated by 604. By way of example, the patterned layer can include a surface structure pattern configured to provide an increased contact area in response to wear. For example, the cured formulation can be extruded or calendered into a sheet. The panel can be stamped, engraved or integrally patterned or any combination of these methods to provide a patterned surface structure. In another exemplary embodiment, the formulation can be extruded or calendered onto a negative surface comprising a negative pattern (where a negative surface is applied to form a pattern of patterned layers). As illustrated by 606, the formulation can be cured after the patterned layer is formed from the uncured formulation. In the case of platinum catalyzed polyoxo, the formulation and the patterned layer formed therefrom can be heated and thus thermally cured. In alternative embodiments, a catalyst system that reacts to actinic radiation can be used. Typical conditions for curing are 5 minutes at 350 °F. A similar method can be carried out using thermoplastic polymer formulations. For example, the thermoplastic polymer formulation can be blended with the abrasive particles and optional reinforcing particles. The blending can be carried out in an extruder or a heat blender. The blending formulation comprising the polymer formulation, the abrasive particles and the reinforcing particles can be extruded and patterned. For example, a surface pattern can be formed in the surface of the extruded layer of the 1228l3.doc -24-1337915 blending formulation using a print, roll or other patterning technique. In a particular example, the blending formulation can be extruded onto a negative patterned mold. The blending formulation can be cooled to form an abrasive layer. An adhesive or fastener layer can be added to form an abrasive product. Alternatively, this method can be modified for use with thermoplastic vulcanizates. While embodiments of abrasive articles can be used in a variety of industrial applications, certain embodiments of abrasive articles are advantageous for use in the surface of the optical media repair industry. For example, a pre-polished process can be used to grind a treated surface such as an optical media or painted surface. Pre-polished is typically performed using coarse abrasive articles and typically removes large surface defects leaving a matte finish. In an exemplary embodiment, the pre-polished surface is further ground using an abrasive article having a particle size smaller than that of the coarse abrasive article. For example, the pre-polished surface can be further ground using an abrasive article formed from the above formulation. The formulation may include a polymer formulation, a oxidizing agent reinforced particle, and an abrasive particle. • In another example, the pre-polished surface can be further ground using an abrasive article comprising a layer having a surface pattern configured to increase surface area with wear. This layer can include polymer formulations and abrasive particles. The abrasive article can be free of backing. After grinding, the ground surface can be polished or polished. For example, the ground surface can be polished or polished with a wool enamel or foam pad. Polished or polished surfaces typically have desirable roughness and gloss. In a particular embodiment, the abrasive article can be used to repair optical media such as cd or DVD. For example, a CD or DVD rental agency or resale 122813.doc -25-1337915 can receive used optical media. In an example, the institution can receive optical media via a store. In another example, the institution can receive the optical media via mail. The abrasive article formed by the above may be ground or DVC). In a special example, the abrasive article does not include a backing layer. In another example, the abrasive article can comprise a pressure sensitive adhesive surface. Can be cleaned and polished or dVD. After iW, a CD or DVD can be provided for subsequent use, such as re-leasing or selling. 3 sheep 5, these abrasive objects are suitable for use without subsequent coating process

之方法,且用研磨物件進行研磨可賦予拋光表面耐污性或 耐灰塵性。 研磨物件之特定實施例在使用時有利地提供經改良之表 面特性。舉例而·r,研磨物件之特定實施例之使用可展現 經研磨表面之粗糙度及光澤之改良。舉例而言,光澤效能 可定義為經使用研磨物件處理之表面的平均光澤。可首先 用購自3M之3M 260L Pl500打磨或預打磨新塗漆金屬表面 上之2呎χ4呎之區域。該預打磨通常產生具有如使用卜The method, and grinding with the abrasive article, imparts stain resistance or dust resistance to the polished surface. Particular embodiments of the abrasive article advantageously provide improved surface characteristics when used. For example, the use of a particular embodiment of an abrasive article can exhibit an improvement in the roughness and gloss of the ground surface. For example, gloss performance can be defined as the average gloss of the surface treated with the abrasive article. The 2呎χ4呎 area on the newly painted metal surface can be first ground or pre-polished with a 3M 260L Pl500 from 3M. The pre-polished usually produces

Federal Perthometer M2所量測之78微吋與9微吋之間的平 均粗輪度(Ra)之表面。使用待測試之研磨物件將經預打磨 之塗漆表面打磨1分鐘。量測平均粗糙度及6〇度光澤 (TriC〇r-system2MiCr〇 TH-G丨oss光澤計)。光澤效能^上述 程序之後的經打磨物件之平均光澤。研磨物件之^定實施 例可產生根據60°之光澤或反射率所量 如至少約26或至少約28_5之平均光澤效 程度上取決於磨粒之粒徑。舉例而言 J400或更南)可產生小於20之光澤, 測之至少約25,諸 旎。光澤效能很大 ,車父粗之磨粒(如 而極細之磨粒(如 122813.doc -26- 1337915 J3000)可產生6〇之光澤。當 网樣本之間的粒徑一致時,黏 合劑調配物及增強顆粒可影塑出 知警先澤效能。另外,粗糙度效 能定義為經以上述方式處理之矣 &lt;表面的平均粗糙度(Ra)。如 以微吋為單位所量測,研磨物株 君物件之特定實施例可展現不大 於約3.5,諸如不大於約31或其 乂爸至不大於約2.6之粗糙度效 厶h 在另-實例中,粗棱度指數及移除指數可基於研磨物件 對丙烤酸樹脂薄板之效能來定義。將研磨產品連接至壓力 ㈣uuuhinis®M偏心砂磨機。在經3M 26〇L 15〇〇預 打磨之6塊丙烯酸樹脂板上打磨產品。總打磨時間為3分 鐘^每塊板30秒鐘。在30秒鐘之後’量測丙稀酸樹脂板之 重$損失及以微吋為單位量測之表面粗糙度Ra。移除指數 定義為6塊丙烯酸樹脂板之累積重量損失且粗糙度指數定 義為第一塊丙烯酸樹脂板之平均粗糙度Ra。詳言之,如以 微吋為單位所量測,研磨產品之粗糙度指數可不大於 6.0,諸如不大於5.0,不大於4〇或甚至不大於3〇。在另一 實例中,如以公克為單位所量測,移除指數可為至少約 0.1 ’諸如至少約0·2,至少約〇 3或甚至至少約〇 5。 實例 實例1 里測由以聚矽氧為主之調配物形成之層的機械特性。調 配物係藉由混合E】ast〇sH⑧3003 LR50液體聚石夕氧部分六及 B(購自Wacker Silicone)與以調配物之總重量計約60 wi%之 奴化石夕研磨粒(購自Nanko)而形成。Elastosil® 3003 I22813.doc -27· 1337915 LR5〇為兩部分之液體裝矽氧,#包括約33重量%之估計含 ϊ的預混&amp;之—氡化矽增強物。此對應於整個調配物中約 13重量。/。之二氧化妙。無研磨粒之丨⑧^^5〇具 有在10,之剪切速率下(DIN 53 019)約360,000 Cps之黏 度,且在無研磨粒存在之情況下固化時’具有約丨〇 6 Mpa 之拉伸強度及520%之伸長率(DIN 53 5〇4 S1)。使調配物在 加熱模具中於175。〇下在壓力下固化5分鐘。 固化調配物展現約7.76 MPa(1126 psi)之拉伸強度及約 137%之斷裂伸長率(ASTM D 412)。另外固化調配物展 現約7.22 MPa (1 048 psi)之100%模數及83之肖氏A硬度。 實例2 將兩種無背層研磨樣本與購自3M之Trizact 443SA P3000 進行比較。樣本1係由包括Wacker® Silicone之Elastosil® 3003 LR50及65 wte/。之WA800氧化鋁研磨粒之調配物形成 且包括結構性稜錐之圖案,該等稜錐具有邊為5〇〇微米之 正方形底及在表面以上約2 5 0微米之高度。在經約4 5分鐘 之循環時間加熱至約350T並冷卻至約100°F之模具中使樣 本1固化。樣本2係由包括Wacker® Silicone之Elastosil® 3003 LR50及60 wt%之J800碳化矽研磨粒之調配物以上述 方式製備。The average coarse wheel (Ra) surface between 78 micro 吋 and 9 吋 measured by the Federal Perthometer M2. The pre-polished painted surface was sanded for 1 minute using the abrasive article to be tested. The average roughness and 6-degree gloss were measured (TriC〇r-system 2 MiCr〇 TH-G丨oss gloss meter). Gloss Efficacy ^ The average gloss of the polished article after the above procedure. The embodiment of the abrasive article can produce an amount of gloss or reflectance of 60°, such as at least about 26 or at least about 28_5, depending on the particle size of the abrasive particles. For example, J400 or more) can produce a gloss of less than 20, measured at least about 25, 诸. Gloss is very effective, the father's coarse abrasive particles (such as the extremely fine abrasive particles (such as 122813.doc -26- 1337915 J3000) can produce a gloss of 6 。. When the particle size between the mesh samples is the same, the adhesive is blended The material and the reinforced particles can be used to shape the effectiveness of the police. In addition, the roughness efficiency is defined as the average roughness (Ra) of the surface treated by the above method. If measured in micro-twist, grinding A particular embodiment of the article can exhibit a roughness effect of no greater than about 3.5, such as no greater than about 31 or its dad to no greater than about 2.6. In another example, the coarseness index and the removal index can be Based on the effectiveness of the abrasive article on the acrylic resin sheet. Connect the abrasive product to a pressure (iv) uuuhinis® M eccentric sander. Polish the product on 6 acrylic plates pre-polished with 3M 26〇L 15〇〇. The grinding time is 3 minutes ^ 30 seconds per plate. After 30 seconds, the weight loss of the acrylic resin sheet and the surface roughness Ra measured in micrometers are measured. The removal index is defined as 6 Cumulative weight loss and roughness of block acrylic plate The number is defined as the average roughness Ra of the first acrylic resin plate. In detail, the roughness index of the ground product may be not more than 6.0, such as not more than 5.0, not more than 4 〇 or even as measured in micro 吋. Not greater than 3. In another example, the measurement may be at least about 0.1' such as at least about 0.2, at least about 〇3, or even at least about 〇5, as measured in grams. Example 1 The mechanical properties of the layer formed by the polyoxo-based formulation were measured by mixing E]ast〇sH83003 LR50 liquid poly-stone part 6 and B (purchased from Wacker Silicone) with the formulation. The total weight is about 60 wi% of the sulphate granules (purchased from Nanko). Elastosil® 3003 I22813.doc -27· 1337915 LR5〇 is a two-part liquid containing oxygen, #includes about 33% by weight It is estimated that the cerium-containing premixed &amp; 氡 矽 矽 矽 。 。 。 。 。 。 。 。 。 。 。 。 。 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约 约Viscosity at a shear rate (DIN 53 019) of approximately 360,000 Cps and in the absence of abrasive particles In the case of curing, it has a tensile strength of about M6 Mpa and an elongation of 520% (DIN 53 5〇4 S1). The formulation is allowed to cure in a heated mold at 175 for 5 minutes under pressure. The cured formulation exhibited a tensile strength of about 7.76 MPa (1126 psi) and an elongation at break of about 137% (ASTM D 412). Additionally, the cured formulation exhibited a 100% modulus of about 7.22 MPa (1 048 psi) and 83 Shore A hardness. Example 2 Two backless ground samples were compared to 3M Trizact 443SA P3000. Sample 1 consisted of Elastosil® 3003 LR50 and 65 wte/ including Wacker® Silicone. The formulation of the WA800 alumina abrasive particles is formed and includes a pattern of structural pyramids having a square bottom with a side of 5 microns and a height of about 250 microns above the surface. Sample 1 was cured in a mold which was heated to about 350 T over a period of about 45 minutes and cooled to about 100 °F. Sample 2 was prepared in the manner described above by a formulation comprising Wlaser® Silicone's Elastosil® 3003 LR50 and 60% by weight of J800 cerium carbide abrasive particles.

為測試樣本之效能,將新塗漆蓋罩之部分用3M 260L P 1500預打磨至約7.8微吋與約9.〇微吋之間的平均粗糙度 (Ra)。使用樣本!或樣本2或比較樣本之一打磨該等部分歷 時1分鐘。表1說明樣本之粗糙度效能及光澤效能D I228I3.doc •28· 1337915 表1 ·粗糙度及光澤效能 樣本1 樣本2 比較樣本-3M之 Trizact Ρ30ΩΠ 粗糙度(微吋) 3.3 3.4 3.3 光澤效能(%) 28.9 26.1 13.5 對於樣本1 '樣本2或比較樣本在表面中均未觀察到缺 陷。與3M之Trizact P3000相比,樣本】及樣本2均展現類似 之粗糙度效能。然而,樣本1及樣本2展現比比較實例約大 100%之經改良光澤效能。 實例3 使用不同增強二氧化矽負載製備兩種無背層研磨樣本。 樣本3係由包括 Wacker® Silicone之 Elastosil® 3 003 LR50 及 60 wt%之J800碳化矽研磨粒之調配物以上述方式製備。樣 本3含有約13°/。之發煙二氧化矽。樣本4係藉由混合dmS-V31乙烯基末端聚二甲基矽氧烷、HMS-301氫化物交聯劑 及SIP 6829.2紐催化劑(各自講自 Geiest, inc, Morrisville, PA)與10 pph Cabosil M5發煙二氧化矽(購自Cabot Corporation)以形成混合物來製備。隨後將混合物與6〇 wt%之J800碳化矽混合。樣本4含有約4%之發煙二氧化 石夕。 在塗有Spies-Hecker清漆且用3M 260L P1500預打磨至在 6.3微吋至7.3微吋範圍内之粗糙度之表面之部分上測試樣 本且與購自3M之Trizact 443SA P3000進行比較。在蓋罩之 相同區域上’各產品之打磨時間均為1分鐘。表2說明樣本 I22813.doc •29- 1337915 之所得粗糙度及光澤效能。 表2.粗糙度及光澤效能 樣本3 樣本4 粗糙度效能 2.4 3.1 _光澤效能 29.2 18.3 '''''' 在經研磨之表面中未觀察到缺陷。樣本3及樣本4均展現 與比較樣本相比經改良之光澤效能。然而,具有較大二氧 化石夕增強劑負載之樣本3展現光澤效能之較大改良及植糖 度效能之改良。 實例4 將無背層研磨樣本與購自3MiTrizact 443SA P3〇〇〇進行 比較。樣本5係由包括 Wacker® Silicone 之 Elastosil® 3003 LR5 0及60 wt%之J800碳化矽研磨粒之調配物形成且包括結 構性稜錐之圖案’其中每線性吋具有45個稜錐。在經約45 分鐘之循環時間加熱至約35〇卞並冷卻至約1〇〇卞之模具中 使樣本5固化。 為測試樣本之效能,將塗有Spies_Hecker清漆之新塗漆 蓋罩之部分用3M 260L P1500預打磨至約7·8微吋與約9.0微 D寸之間的平均粗糙度(Ra) ^隨後,使用樣本5或比較樣本 打磨該等部分歷時丨分鐘。表3說明樣本之粗糙度效能及光 澤效能。 122813.doc 1337915 表3 樣本5 Trizact 443 SA P3000 Ra (u&quot;) 3.9 2.9 60度光澤(%) 24 14 註釋 光面 亞光毛面 樣本5展現比比較產品之光澤效能高的光澤效能。 實例5 將兩種無为層研磨樣本與購自3Μ之Trizact 443SA Ρ3000 進行比較。樣本6及樣本7係由包括Wacker® Silicone之 Elastosil® 3 003 LR5 0及60 wt%之J800碳化石夕研磨粒之調配 物形成且包括結構性棱錐之圖案’其中每線性忖具有4 5個 稜錐。樣本6係經由壓縮成型法形成且樣本7係藉由播壓及 壓印形成。 為測試樣本之效能,將塗有Spies-Hecker清漆之新塗漆 蓋罩之部分用3M 260L P1500預打磨至約7.8微叫·與約9.0微 吋之間的平均粗糙度(Ra)。隨後’使用樣本6或樣本7或比 較樣本之一打磨該等部分歷時1分鐘。表4說明樣本之粗糖 度效能及光澤效能。 表4 樣本6 樣本7 Trizact 443 SA P3000 Ra (υ&quot;) 4.6 4.5 3.3 60度光澤(%) 16 15 11 樣本6及樣本7均展現相對於比較樣本經改良之光澤效 能0 122813.doc 31 1337915 貫例6 將兩種無背層研磨樣本與購自3M之Trizact 443SA P3000 進行比較。樣本8及樣本9係由包括Wacker@ siHcone之 ElaSt〇sil® 3003 lR50及60 wt%之J8〇〇碳化矽研磨粒之調配 物形成。樣本8具有每線性吋包括90個稜錐之表面且樣本9 具有每線性吋具有45個稜錐之圖案。兩樣本均係經由壓縮 成型法形成。 為測試樣本之效能,將塗有Spies_Hecker清漆之新塗漆 蓋罩之部分用3M 260L P1 500預打磨至約7.8微吋與約9.0微 吋之間的平均粗糙度(Ra)。隨後,使用樣本8或樣本9或比 較樣本之一打磨該等部分歷時1分鐘。表5說明樣本之粗糙 度效能及光澤效能。 表5 樣本8 樣本9 Trizact 443 S A P3000 Ra (u&quot;)__ 3.7 4~5 3.4 60度光澤(%) 21 16 11To test the performance of the sample, the portion of the new painted cover was pre-polished with 3M 260L P 1500 to an average roughness (Ra) of between about 7.8 micrometers and about 9. micrometers. Use the sample! Or one of the sample 2 or comparison samples is polished for 1 minute. Table 1 shows the roughness performance and gloss performance of the sample. D I228I3.doc •28· 1337915 Table 1 ·Roughness and gloss efficacy sample 1 Sample 2 Comparison sample -3M Trizact Ρ30ΩΠ Roughness (micro-吋) 3.3 3.4 3.3 Gloss performance ( %) 28.9 26.1 13.5 For sample 1 'sample 2 or comparative sample, no defects were observed in the surface. Both the sample and the sample 2 exhibited similar roughness performance compared to the 3M Trizact P3000. However, Sample 1 and Sample 2 exhibited improved gloss performance about 100% greater than the comparative example. Example 3 Two non-backed abrasive samples were prepared using different enhanced cerium oxide loadings. Sample 3 was prepared in the manner described above by a formulation comprising Wlaser® Silicone's Elastosil® 3 003 LR50 and 60 wt% J800 tantalum carbide abrasive particles. Sample 3 contains about 13°/. The fuming cerium oxide. Sample 4 was prepared by mixing dmS-V31 vinyl-terminated polydimethyloxane, HMS-301 hydride crosslinker, and SIP 6829.2 catalyst (each from Geiest, inc, Morrisville, PA) with 10 pph Cabosil M5. Fuming cerium oxide (available from Cabot Corporation) was prepared to form a mixture. The mixture was then mixed with 6 wt% of J800 niobium carbide. Sample 4 contained about 4% of the fumed silica dioxide. Samples were tested on a portion coated with a Spies-Hecker varnish and pre-polished with 3M 260 L P1500 to a roughness in the range of 6.3 micrometers to 7.3 micrometers and compared to Trizact 443SA P3000 purchased from 3M. On the same area of the cover, the grinding time of each product was 1 minute. Table 2 illustrates the resulting roughness and gloss performance of the sample I22813.doc •29-1337915. Table 2. Roughness and Gloss Efficacy Sample 3 Sample 4 Roughness Efficacy 2.4 3.1 _ Gloss Efficacy 29.2 18.3 '''''' No defects were observed in the ground surface. Both Sample 3 and Sample 4 exhibited improved gloss performance compared to the comparative samples. However, Sample 3 with a larger concentration of sulphur dioxide enhancer exhibited a greater improvement in gloss performance and an improvement in the efficiency of the saccharide. Example 4 A backless ground sample was compared to that obtained from 3MiTrizact 443SA P3. Sample 5 was formed from a formulation comprising Wlaser® Silicone's Elastosil® 3003 LR50 and 60 wt% J800 tantalum carbide abrasive particles and including a pattern of structural pyramids with 45 pyramids per linear tantalum. Sample 5 was cured in a mold which was heated to about 35 Torr over a period of about 45 minutes and cooled to about 1 Torr. To test the performance of the sample, the portion of the new painted cover coated with Spies_Hecker varnish was pre-polished with 3M 260L P1500 to an average roughness (Ra) between about 7.8 micrometers and about 9.0 microDs. ^ Subsequently, Use Part 5 or a comparison sample to polish the parts for a few minutes. Table 3 shows the roughness performance and gloss performance of the samples. 122813.doc 1337915 Table 3 Sample 5 Trizact 443 SA P3000 Ra (u&quot;) 3.9 2.9 60 degree gloss (%) 24 14 Note Glossy matte matte Sample 5 exhibits a gloss performance that is higher than the gloss performance of the comparative product. Example 5 Two non-layered ground samples were compared to Trizact 443SA® 3000 purchased from 3Μ. Sample 6 and Sample 7 were formed from a formulation comprising Wlaser® Silicone's Elastosil® 3 003 LR50 and 60 wt% J800 carbonized carbide abrasive particles and including a pattern of structural pyramids with 45 ridges per linear enthalpy Cone. Sample 6 was formed by compression molding and sample 7 was formed by weaving and embossing. To test the performance of the sample, the portion of the new painted cover coated with Spies-Hecker varnish was pre-polished with 3M 260L P1500 to an average roughness (Ra) of between about 7.8 micro-injections and about 9.0 micro-twist. These portions were then polished using Sample 6 or Sample 7 or one of the comparative samples for 1 minute. Table 4 shows the crude sugar performance and gloss performance of the samples. Table 4 Sample 6 Sample 7 Trizact 443 SA P3000 Ra (υ&quot;) 4.6 4.5 3.3 60 degree gloss (%) 16 15 11 Both sample 6 and sample 7 exhibit improved gloss performance relative to the comparative sample. 0 122813.doc 31 1337915 Example 6 Two backless ground samples were compared to 3M Trizact 443SA P3000. Samples 8 and 9 were formed from a formulation comprising Wacker@ siHcone's Ela St〇sil® 3003 lR50 and 60 wt% of J8 tantalum carbide abrasive particles. Sample 8 has a surface comprising 90 pyramids per linear 且 and sample 9 has a pattern of 45 pyramids per linear 吋. Both samples were formed by compression molding. To test the efficacy of the sample, the portion of the new painted cover coated with Spies_Hecker varnish was pre-polished with 3M 260L P1 500 to an average roughness (Ra) of between about 7.8 microcubes and about 9.0 microtwist. Subsequently, the portions were polished using sample 8 or sample 9 or one of the comparative samples for 1 minute. Table 5 shows the roughness performance and gloss performance of the samples. Table 5 Sample 8 Sample 9 Trizact 443 S A P3000 Ra (u&quot;)__ 3.7 4~5 3.4 60 degree gloss (%) 21 16 11

樣本8展現相對於樣本9及比較樣本經改良之光澤效能。 實例7 將二種無背層研磨樣本與購自31VI之Trizact 443SA P3000 進行比較。樣本1 0、樣本Π及樣本1 2係由包括Wacker® Silicone 之 Elastosil® 3003 LR50 及 60 wt°/。之 J800 碳化石夕研 磨粒之調配物形成。樣本1 〇具有每線性吋90個棱錐之圖 案,樣本11具有每線性吋45個棱錐之圖案,且樣本;[2具有 122813.doc -32- 1337915 每吋35條線之隨機三螺旋圖案。 為測試樣本之效能,將塗有Spies-Hecker清漆之新塗漆 盖罩之部分用3M 260L P1 500預打磨至約7.8微吋與約9.0微 °寸之間的平均粗糙度(Ra)。隨後,使用樣本1 0、樣本U或 樣本12或比較樣本之一打磨該等部分歷時1分錢。表6說明 樣本之粗糙度效能及光澤效能。 表6 樣本10 樣本11 樣本12 Trizact 443S A P3000 Ra (u&quot;) 3.8 3.8 3.2 3.1 60度光澤(%) 18 17 26 14 往釋 有光澤 且均一 有光澤 且均一 極有光澤, 但模型化 無光澤 且均一 樣本12展現相對於樣本10及樣本11及比較樣本經改良之 光澤效能。 實例8 將兩種無背層研磨樣本與購自3M之Trizact 443SA P3000 進行比較。樣本13及樣本14係由包括Wacker® Silicone之 Elastosil® 3003 LR50及60 wt%之J800碳化矽研磨粒之調配 物形成。樣本1 3具有每線性忖包括4 5個稜錐之表面且樣本 14具有每線性吋具有125個嵌塊之圖案。 為測試樣本之效能,將塗有Spies-Hecker清漆之新塗漆 蓋罩之部分用3M 260L P1 500預打磨至約7_8微吋與約9.0微 吋之間的平均粗糙度(Ra)。隨後,使用樣本13或樣本丨4或 比較樣本之一打磨該等部分歷時1分鐘。表7說明樣本之粗 縫度效能及光澤效能。 122813.doc -33- 表7 樣本13 樣本14 Trizact 443 S A P3000 Ra iu&quot;) 2.6 2,5 3.2 60度光澤(%) 35 36 11.7 註釋 光面 光面 亞光毛面 1337915 樣本13及樣本14展現相對於比較樣本經改良之可比較光 澤效能。 實例9 將兩種無背層研磨樣本與購自3M之Trizact 443SA P3000 進行比較。樣本15係由包括Wacker® Silicone之Elastosil® 3003 LR50及60 wt%之J800碳化矽研磨粒之調配物形成, 其中每線性吋具有45個稜錐。樣本16係由包括Lotryl 29-Ma-03及75 wt%之J800碳化矽研磨粒之調配物形成,其中 每線性吋具有45個稜錐。 為測試樣本之效能,將塗有Spies-Hecker清漆之新塗漆 蓋罩之部分用3M 260L P1500預打磨至約7.8微吋與約9.0微 忖之間的平均粗糙度(Ra)。隨後,使用樣本15或樣本16或 比較樣本之一打磨該等部分歷時1分鐘。表8說明樣本之粗 輪度效能及光澤效能。 表8 樣本15 樣本16 Trizact 443 S A P3000 Ra (u&quot;) 2.7 3.7 2.8 60度光澤 (%) 40 20 24 註釋 光面 模型化 亞光毛面 1228l3.doc -34 · 1337915 樣本1 5展現相對於樣本16及比較樣本經改良之光澤效 能。 實例1 0 製備無背層研磨樣本並對其進行測試以測定如上定義之 移除指數及粗縫度指數。表示為LSR2之彼等樣本係由聚 矽氧油(100 g DMS-V31乙烯基末端聚矽氧與35 g HMS_ 3〇1氫化物交聯劑及適合iPt催化劑)製成。將液體與各種 1之發煙二氧化石夕及J800研磨粒混合並使其固化以形成無 背層研磨物件。表9說明樣本之移除指數及粗糙度指數。 表9Sample 8 exhibited improved gloss performance relative to sample 9 and comparative samples. Example 7 Two backless ground samples were compared to Trizact 443SA P3000 from 31VI. Sample 10, sample Π and sample 1 2 are from Elastosil® 3003 LR50 and 60 wt°/ including Wacker® Silicone. The J800 carbonized stone Xiyan abrasive composition is formed. Sample 1 〇 has a pattern of 90 pyramids per linear ,, sample 11 has a pattern of 45 pyramids per linear ,, and a sample; [2 has a random triple helix pattern of 122813.doc -32 - 1337915 per 35 lines. To test the performance of the sample, the portion of the new painted cover coated with Spies-Hecker varnish was pre-polished with 3M 260L P1 500 to an average roughness (Ra) of between about 7.8 microcubes and about 9.0 microcubits. Subsequently, the parts are polished using sample 10, sample U or sample 12 or one of the comparative samples for a period of 1 cent. Table 6 shows the roughness performance and gloss performance of the samples. Table 6 Sample 10 Sample 11 Sample 12 Trizact 443S A P3000 Ra (u&quot;) 3.8 3.8 3.2 3.1 60 degree gloss (%) 18 17 26 14 The release is shiny and uniform, shiny and uniform, but the model is dull. And the same as this 12 shows improved gloss performance relative to sample 10 and sample 11 and comparative samples. Example 8 Two backless ground samples were compared to 3M Trizact 443SA P3000. Sample 13 and Sample 14 were formed from a formulation comprising Wacker® Silicone's Elastosil® 3003 LR50 and 60 wt% J800 tantalum carbide abrasive particles. Sample 13 has a surface comprising 45 pyramids per linear 且 and sample 14 has a pattern of 125 tiles per linear 吋. To test the efficacy of the sample, the portion of the new painted cover coated with Spies-Hecker varnish was pre-polished with 3M 260 L P1 500 to an average roughness (Ra) of between about 7-8 microcubits and about 9.0 microtwist. Subsequently, the portions are polished using sample 13 or sample 丨4 or one of the comparative samples for 1 minute. Table 7 shows the coarseness and gloss performance of the samples. 122813.doc -33- Table 7 Sample 13 Sample 14 Trizact 443 SA P3000 Ra iu&quot;) 2.6 2,5 3.2 60 degree gloss (%) 35 36 11.7 Note Glossy matte matte surface 1337915 Sample 13 and sample 14 show The improved gloss is comparable to the comparative sample. Example 9 Two backless ground samples were compared to 3M Trizact 443SA P3000. Sample 15 was formed from a formulation comprising Wlaser® Silicone's Elastosil® 3003 LR50 and 60 wt% J800 tantalum carbide abrasive particles, each having 45 pyramids. Sample 16 was formed from a formulation comprising Lotryl 29-Ma-03 and 75 wt% of J800 cerium carbide abrasive particles, with 45 pyramids per linear enthalpy. To test the efficacy of the sample, the portion of the new painted cover coated with Spies-Hecker varnish was pre-polished with 3M 260 L P1500 to an average roughness (Ra) of between about 7.8 micro-twist and about 9.0 micro-twist. Subsequently, the portions are sanded using sample 15 or sample 16 or one of the comparative samples for 1 minute. Table 8 shows the coarse roundness performance and gloss performance of the sample. Table 8 Sample 15 Sample 16 Trizact 443 SA P3000 Ra (u&quot;) 2.7 3.7 2.8 60 degree gloss (%) 40 20 24 Note Glossy modeled matte matte 1228l3.doc -34 · 1337915 Sample 1 5 shows relative to the sample 16 and compare the improved gloss performance of the sample. Example 10 A backless ground sample was prepared and tested to determine the removal index and the roughness index as defined above. The samples, designated LSR2, were made from polyoxygenated oil (100 g DMS-V31 vinyl terminated polyfluorene with 35 g HMS_3〇1 hydride crosslinker and suitable for iPt catalyst). The liquid is mixed with various types of fumed silica dioxide and J800 abrasive particles and cured to form a backless abrasive article. Table 9 illustrates the sample removal index and roughness index. Table 9

表9大體說明填料顆粒負載之增加降低粗糙度指數,同 時對移除指數幾乎無影響。 實例11 製備無背層研磨樣本並對其進行測試以測定如上定義之 移除指數及粗糙度指數。樣本係由各種熱塑性材料及熱固 性材料及不同s:及類型之研磨粒製備。表丨〇說明由各種調 配物形成之研磨產品之移除指數及粗糙度指數。 122813.doc -35· 1337915Table 9 generally shows that the increase in filler particle loading reduces the roughness index and has little effect on the removal index. Example 11 A backless ground sample was prepared and tested to determine the removal index and roughness index as defined above. The samples were prepared from a variety of thermoplastic and thermoset materials and abrasive granules of different s: and types. The table indicates the removal index and roughness index of the ground product formed from various formulations. 122813.doc -35· 1337915

表ίο 樹脂 研磨粒 Wt% 研磨粒1 研磨粒2 移除 指數 粗?度 指數 類型 磨粒 類型 磨粒 Elastollan 1180A 60 SiC J800 0.11 2.6 Elastollan 1180A 75 SiC J800 Elvacite 4044 60 SiC J800 0.49 4.0 Evatane 24-03 60 SiC J800 0.00 Ενatane 40-55 60 SiC J800 0.00 Evatane 40-55 70 SiC J800 0.03 2.6 Evatane 40-55 75 SiC J800 0.01 2.3 Evatane 40-55 80 SiC J400 SiC J3000 0.54 5.2 Evatane 40-55 80 SiC J600 Alum WA6000 0.29 2.9 Lotader 3430 60 SiC J800 0.13 1.9 Lotader 3430 75 SiC J800 0.25 2.7 Lotader 3430 80 SiC J800 X X Lotader AX 8900 60 SiC J800 0.21 1.7 Lotader AX 8900 75 SiC J800 0.19 1.8 Lotryl 15-MA-03 60 SiC J800 0.09 2.0 Lotryl 29-MA-03 60 SiC J800 0.02 2.0 Lotryl 29-MA-03 70 SiC J800 0.22 2.2 Lotryl 29-MA-03 75 SiC J800 0.37 2.5 Lotryl 29-MA-03 80 SiC J400 SiC J3000 0.42 5.0 Lotryl 29-MA-03 84 SiC J600 Alum WA6000 0.49 3.5 Lotryl 29-MA-03 80 SiC J600 Alum WA6000 0.22 3.0 Lotryl 29-MA-03 80 SiC J600 Alum WA6000 0.28 3.5 Lotryl 29-MA-03 80 SiC J600 0.36 3.6 Lotryl 30-BA-02 60 SiC J800 0.13 2.1 Orevac 18211 60 SiC J800 0.09 2.0 Pebax 2533 60 SiC J800 0.04 3.3 Pebax 2533 75 SiC J800 0.25 3.2 PLA 2002D+Tegomer H-Si 6440 65 SiC J800 0.49 4.5 Riteflex 430 60 SiC J800 0.23 2.3 Riteflex 430 75 SiC J800 0.29 3.4 Elastosil 3003 LR50 60 SiC J800 0.63 2.0 上述標的物應視為係說明性而非限制性的,且所附申請 專利範圍意欲涵蓋在本發明之實質範疇内之所有修改、增 加及其他實施例。因此,在法律所允許之最大程度上,本 發明之範疇由以下申請專利範圍及其均等物之最廣泛玎允 I22813.doc •36- 1337915 許的解釋來確定且不應受前述詳細說明約束或限制 【圖式簡單說明】 ° 圖1包括例示性結構化研磨物件之橫截面圖之說明 圖2及圖3包括例示性結構化研磨物件中 卞甲之呈表面突起圖 案之形式的例示性表面特徵層之說明。 圖4及圖5包括例示性結構化研磨物体夕主 切讦之表面特徵之例示 性橫截面之說明。 圖ό包括說明用於形成例示性結構化研磨物件之例示性 方法之流程圖。 圖7包括例示性結構化研磨物件之橫戴面圖之說明。Table ί Resin Abrasive Grain Wt% Abrasive Grain 1 Abrasive Grain 2 Removal Index Thickness Index Type Abrasive Type Abrasive Elastollan 1180A 60 SiC J800 0.11 2.6 Elastollan 1180A 75 SiC J800 Elvacite 4044 60 SiC J800 0.49 4.0 Evatane 24-03 60 SiC J800 0.00 Ενatane 40-55 60 SiC J800 0.00 Evatane 40-55 70 SiC J800 0.03 2.6 Evatane 40-55 75 SiC J800 0.01 2.3 Evatane 40-55 80 SiC J400 SiC J3000 0.54 5.2 Evatane 40-55 80 SiC J600 Alum WA6000 0.29 2.9 Lotader 3430 60 SiC J800 0.13 1.9 Lotader 3430 75 SiC J800 0.25 2.7 Lotader 3430 80 SiC J800 XX Lotader AX 8900 60 SiC J800 0.21 1.7 Lotader AX 8900 75 SiC J800 0.19 1.8 Lotryl 15-MA-03 60 SiC J800 0.09 2.0 Lotryl 29 -MA-03 60 SiC J800 0.02 2.0 Lotryl 29-MA-03 70 SiC J800 0.22 2.2 Lotryl 29-MA-03 75 SiC J800 0.37 2.5 Lotryl 29-MA-03 80 SiC J400 SiC J3000 0.42 5.0 Lotryl 29-MA-03 84 SiC J600 Alum WA6000 0.49 3.5 Lotryl 29-MA-03 80 SiC J600 Alum WA6000 0.22 3.0 Lotryl 29-MA-03 80 SiC J600 Alum WA60 00 0.28 3.5 Lotryl 29-MA-03 80 SiC J600 0.36 3.6 Lotryl 30-BA-02 60 SiC J800 0.13 2.1 Orevac 18211 60 SiC J800 0.09 2.0 Pebax 2533 60 SiC J800 0.04 3.3 Pebax 2533 75 SiC J800 0.25 3.2 PLA 2002D+Tegomer H-Si 6440 65 SiC J800 0.49 4.5 Riteflex 430 60 SiC J800 0.23 2.3 Riteflex 430 75 SiC J800 0.29 3.4 Elastosil 3003 LR50 60 SiC J800 0.63 2.0 The above subject matter is to be regarded as illustrative and not limiting, and the attached application All modifications, additions, and other embodiments are intended to be included within the scope of the invention. Therefore, to the extent permitted by law, the scope of the invention is determined by the following broad description of the scope of the claims and the equivalents thereof, which are not limited by the foregoing detailed description or Limitations [Simplified Schematic Description] FIG. 1 includes an illustration of a cross-sectional view of an exemplary structured abrasive article. FIG. 2 and FIG. 3 include an exemplary surface feature layer in the form of a surface protrusion pattern of an armor in an exemplary structured abrasive article. Description. Figures 4 and 5 include illustrations of exemplary cross-sections of surface features of an exemplary structured abrasive object. The figure includes a flow chart illustrating an exemplary method for forming an exemplary structured abrasive article. Figure 7 includes an illustration of a cross-sectional view of an exemplary structured abrasive article.

【主要元件符號說明】 D 100 研磨物件 102 研磨層 104 黏著層 106 扣件板 108 突出結構 200 圖案 202 研磨層 204 研磨結構 300 圖案 302 研磨層 304 研磨結構 400 研磨結構 402 寬度 122813.doc -37- 1337915[Main component symbol description] D 100 abrasive article 102 abrasive layer 104 adhesive layer 106 fastener plate 108 protruding structure 200 pattern 202 abrasive layer 204 abrasive structure 300 pattern 302 abrasive layer 304 abrasive structure 400 abrasive structure 402 width 122813.doc -37- 1337915

404 接觸面積 406 垂直高度 408 水平面 500 橫截面 502 表面 504 接觸表面 702 研磨層 704 黏著層 708 表面特徵404 contact area 406 vertical height 408 horizontal plane 500 cross section 502 surface 504 contact surface 702 abrasive layer 704 adhesive layer 708 surface characteristics

122813.doc -38122813.doc -38

Claims (1)

13379151337915 第096125711號專利申請案 - 中文申請專利範圍替換本(99年7月) 十、申請專利範圍: 1. 一種無背層研磨物件,其包含: V、有第主表面及第二主表面之研磨層,該研磨層係 自行支樓4第-主表面界^ _組突起,該研磨層係由 聚合物調配物及研磨粒形成; 直接與該第二主表面接觸之黏著層,該黏著層包含黏 著劑;及 直接與該黏著層接觸之扣件層。Patent Application No. 096125711 - Chinese Patent Application Substitution (June 99) X. Patent Application Range: 1. A non-backed abrasive article comprising: V, having a primary surface and a second major surface a layer, the abrasive layer is a first-main surface boundary of the self-supporting building 4, the polishing layer is formed by a polymer formulation and abrasive particles; an adhesive layer directly contacting the second major surface, the adhesive layer comprising Adhesive; and a fastener layer that is in direct contact with the adhesive layer. 2.如明求項i之無背層研磨物件,其中該聚合物調配物包 括熱塑性聚合物。 其中該聚合物調配物包 其中該聚合物調配物包 其中該聚合物調配物具 其中該聚矽氧樹脂係由 3.如請求項丨之無背層研磨物件 括一稀彈性體。 4.如請求項1之無背層研磨物件, 括聚矽氧樹脂。 5.如清求項1之無背層研磨物件, 有至少約50%之斷裂伸長率。 6·如4求項4之無背層研磨物件, 液體聚矽氧樹脂形成。 7·如請求項1之無背層研磨物件,其中該研 括增強顆粒。 埯步包 8.::請求項7之無背層研磨物件,其中該增 係至少約3 wt%。 3置 其中該等研磨粒包括碳 9.如听求項1之無背層研磨物件 化石夕〇 122813-990705.doc 1337915 ίο11 12 13. 14. 15. 16. 17. 18. 19. 如請求項丨之無背層研磨物件 約30 wt°/。之該等研磨粒。 如凊求項1之無背層研磨物件 約100%之斷裂伸長率。 如清求項丨之無背層研磨物件, 於約5〇〇密耳之厚度。 如請求項12之無背層研磨物件 350密耳。 如請求項1之無背層研磨物件 圖案。 如請求項1之無背層研磨物件, 斜之表面突起。 其中該研磨層包括至少 其中該研磨層具有至少 其中該研磨層具有不大 其中該厚度係不大於約 其中該組突起排列成一 其中該組突起為側璧傾 一種研磨物件,其包含: 具有第主側面及第二主側面之研磨層該第一主 側面界定-組自該研磨物件之第一表面伸出之突起該 研磨層係由聚合物調配物及研磨粗形成;及:直接與該第二主側面接觸之黏著層,姉著層包含 黏著劑,該黏著層界定該研磨物件之第二外表面。如請求項16之研磨物件,其中該聚合物調配物具有至少 約50°/。之斷裂伸長率。如請求項16之研磨物件’其中該聚合物調配物包括熱塑 性聚合物。 如請求㈣之研磨物件,其中該聚合物調配物包括聚石夕 氧樹脂。 122813-990705.doc 20. 20. 如請求項19之研磨物件, 矽氧樹脂形成。 如睛求項1 6之研磨物件, 之斷裂伸長率。 如請求項1 6之研磨物件 5〇〇密耳之厚度。 如請求項16之研磨物件, 如請求項1 6之研磨物件, 面突起。 其中該聚矽氧樹脂係由液體聚 21. 22. 23. 24. 25. 26. 27. 28. 29. 30. 其中該研磨層具有至少約1〇0% ’其中該研磨層具有不大於約 其中該組突起排列成一圖案。 其中5亥組犬起為側壁傾斜之表 —種研磨物件,其包含: 具有界定該研磨層之主要表面的—列突起之自行支揮 研磨層,該研磨層係由聚合物及分散於該聚合物中之= 磨粒形成,該研磨層具有不大於約500密耳之厚度节 突起具有不大於20密耳之厚度;且 X 其中該研磨物件無背層。 如請求項25之研磨物件,其中該厚度係不大於約35〇密 耳。 如請求項25之研磨物件,其進一步包含直接與該研磨層 接觸之黏著層。 如請求項27之研磨物件,其中該黏著層形成經組態用以 將該研磨物件連接至一研磨機之壓敏性表面。 如請求項27之研磨物件,其進一步包含直接與該點著層 接觸之扣件層。 一種修復光學媒體之方法,該方法包含: 1228I3-990705.doc 1337915 接收經使用的光學媒體; 使用研磨物件研磨該用舊的光學媒體,該無背層研磨 物件包含具有第一主表面及第二主表面之自行支撐研磨 層,該研磨層係由聚合物及分散於該聚合物中之研磨粒 形成,該自行支撐研磨層具有不大於約5〇〇密耳之厚 度,該無背層研磨物件進一步包含直接與該研磨層之第 一主表面接觸之黏著層,該黏著層包含黏著劑,該黏著 層形成該研磨物件之外表面,該第一主表面界定一組突 起; 提供該光學媒體用於後續使用。 31. 如請求項30之方法,其中該無背層研磨物件包括直接與 δ亥研磨層之該第二主表面接觸之黏著層。 32. 如請求項31之方法,其中該無背層研磨物件包括直接與 該黏著層接觸之扣件層。 33. —種研磨物件,其係由固化調配物形成,該調配物包含 液體聚矽氧橡膠、二氧化矽增強顆粒及研磨粒。 34. 如請求項33之研磨物件,其中該二氧化矽增強顆粒包括 發煙二氧化石夕。 35. 如請求項33之研磨物件,其中該調配物包含至少約3 wt°/。之該二氧化矽增強顆粒。 3 6.如請求項35之研磨物件,其中該調配物包含至少約ι〇 wt%之該二氧化矽增強顆粒。 37.如請求項33之研磨物件,其中該等研磨粒係選自由氮化 物、碳化物、氧化物或其摻合物組成之群。 122813-990705.doc 1337915 38. 如請求項37之研磨物件,其中該等研磨粒包括碳化物。 39. 如請求項38之研磨物件,其中該碳化物係選自由碳化 夕免化觸、奴化鹤及碳化欽組成之群。 4〇·如請求項39之研磨物件,其中該碳化物包括碳化石夕。 41. 如請求項37之研磨物件,其中該等研磨粒包括氮化物。 42. 如請求項41之研磨物件,其中該氮化物係選自由立方氮 化硼及氮化矽組成之群。 43. 如請求項37之研磨物件,其中該等研磨粒包括氧化物。 44·如請求項43之研磨物件,其令該氧化物係選自由以下各 物組成之群:二氧化石夕、氧化結、氧化錯、氧化錯/氧化 紹、二氧化鈽、二氧化斜、 軋化鈦氧化錫、氧化鐵及氧化鉻。 45·如請求項33之研磨物件’其中該等研磨粒係選自由以下 各物組成之群:二氧化石々、备&amp; &gt; , 夕乳化鋁(熔融或燒結)、氧化 鍅、氧化锆/氧化鋁、碳彳b &gt;、 厌化矽石榴石、金剛石、立方氮 化硼、氮化矽、二氧化舖、_备 飾一乳化鈦 '二硼化鈦、碳化 棚、氧化錫、碳化鎮、础几# &quot; ^杈化鈦、氧化鐵、氧化鉻、燧 石、金剛砂及其任何組合。 46·如請求項33之研磨物件’其中該調配物包括至少約30 wt%之該等研磨粒。 47.如請求項46之研磨物件 wt%之該等研磨粒。 其中s亥調配物包括至少約45 48.如請求項47之研磨物件,其中 兵〒。亥調配物包括至少約5 5 wt%之該等研磨粒。 49·如請求項33之研磨物件’其中該液體聚石夕氧橡膠係由兩 122813-990705.doc 1337915 部分聚矽氧橡膠形成,其中—部分包括交聯劑。 50. 51. 52. 53. 54. 55. 56. 57. 58. 59. 60. 61. 如請求項49之研磨物件,其中該交聯劑具有聚矽氧主 鍵。 如凊求項33之研磨物件,其中該固化調配物具有至少約 100%之斷裂伸長率。 如請求項5 1之研磨物件,其中該斷裂伸長率為至少約 120%。 如請求項52之研磨物件,其中該斷裂伸長率為至少約 135%。 其中該固化調配物具有不大於 其中該固化調配物具有不大於 其中該拉伸模數不大於約76 如請求項33之研磨物件, 75之肖氏(Shore)D硬度。 如請求項33之研磨物件, 約8.0 MPa之拉伸模數。 如請求項5 5之研磨物件 MPa。 如請求項33之研磨物件,其中該固化調配物具有至少約 7.0 MPa之拉伸強度。 如請求項33之研磨物件’其中該拉伸強度為至少約7.5 MPa 〇 如請求項33之研磨物件,其中該研磨物件係里研磨板之 形式且其中該研磨物件無背層。 如請求項33之研磨物件,其中該研磨物件係呈具有一主 表面之板形式,其中該主表面具有表面突起之一组合。 如請求項60之研磨物件,其中該表面突起之組合係排列 J22813-990705.doc I337915 成一圖案。 62. 如請求項61之研磨物件 之表面突起。 63. 如請求項61之研磨物件 之表面突起。 其中”亥等表面突起為側壁傾斜 其中該等表面突起為側壁垂直 如請求項33之研磨物件,其進—步包括黏著層β2. The backless ground article of claim i, wherein the polymer formulation comprises a thermoplastic polymer. Wherein the polymer formulation comprises wherein the polymer formulation comprises the polymer formulation wherein the polyoxyxene resin comprises a dilute elastomer as claimed in claim 3. 4. The backless abrasive article of claim 1 comprising a polyoxyn resin. 5. The uncoated abrasive article of claim 1, having an elongation at break of at least about 50%. 6. The non-backed abrasive article of claim 4, formed of a liquid polyoxyn resin. 7. The backless abrasive article of claim 1 wherein the reinforcing particles are included.埯 包 8.:: The backless ground article of claim 7, wherein the buildup is at least about 3 wt%. 3 wherein the abrasive particles comprise carbon 9. The backless abrasive article fossil as recited in claim 1 122813-990705.doc 1337915 ίο11 12 13. 14. 15. 16. 17. 18. 19.无The backless layer of abrasive article is about 30 wt ° /. The abrasive particles. For example, the non-backed abrasive article of Item 1 is about 100% elongation at break. For example, the thickness of the backless layer of the object is about 5 mils. The backless abrasive article of claim 12 is 350 mils. The backless abrasive article pattern of claim 1. If there is no back-grinding object of claim 1, the inclined surface is raised. Wherein the polishing layer comprises at least wherein the polishing layer has at least wherein the polishing layer has a size that is not greater than the thickness of the group of protrusions, wherein the group of protrusions are arranged in a state in which the group of protrusions are laterally inclined, comprising: An abrasive layer of the side surface and the second major side defining the first main side defining a protrusion protruding from the first surface of the abrasive article; the polishing layer being formed by the polymer formulation and the abrasive rough; and: directly and the second The adhesive layer of the main side contact, the squat layer comprising an adhesive, the adhesive layer defining a second outer surface of the abrasive article. The abrasive article of claim 16, wherein the polymer formulation has a minimum of about 50°/. Elongation at break. The abrasive article of claim 16 wherein the polymer formulation comprises a thermoplastic polymer. The abrasive article of claim 4, wherein the polymer formulation comprises a polyoxin. 122813-990705.doc 20. 20. The abrasive article of claim 19, formed of a silicone resin. The elongation at break of the abrasive article of item 16. The thickness of the 5 mil ear as claimed in item 16. The abrasive article of claim 16, such as the abrasive article of claim 16, has a raised surface. Wherein the polyoxynene resin is polymerized from a liquid 21. 22. 23. 24. 25. 26. 27. 28. 29. 30. wherein the abrasive layer has at least about 1% 0% 'where the abrasive layer has no greater than about The set of protrusions are arranged in a pattern. The 5H group of dogs is a table for tilting the side wall - an abrasive article comprising: a self-supporting polishing layer having a column of protrusions defining a major surface of the polishing layer, the polishing layer being polymerized and dispersed in the polymerization In the presence of abrasive particles, the abrasive layer has a thickness of no greater than about 500 mils and the nodal protrusions have a thickness of no greater than 20 mils; and X wherein the abrasive article has no backing layer. The abrasive article of claim 25, wherein the thickness is no greater than about 35 mils. The abrasive article of claim 25, further comprising an adhesive layer in direct contact with the abrasive layer. The abrasive article of claim 27, wherein the adhesive layer forms a pressure sensitive surface configured to attach the abrasive article to a grinder. The abrasive article of claim 27, further comprising a fastener layer in direct contact with the point layer. A method of repairing an optical medium, the method comprising: 1228I3-990705.doc 1337915 receiving an optical medium used; grinding the used optical medium with an abrasive article, the backless abrasive article comprising a first major surface and a second The primary surface self-supports the abrasive layer formed from a polymer and abrasive particles dispersed in the polymer, the self-supporting abrasive layer having a thickness of no greater than about 5 mils, the backless abrasive article Further comprising an adhesive layer directly in contact with the first major surface of the abrasive layer, the adhesive layer comprising an adhesive layer forming an outer surface of the abrasive article, the first major surface defining a set of protrusions; For subsequent use. 31. The method of claim 30, wherein the backless abrasive article comprises an adhesive layer that is in direct contact with the second major surface of the delta-grinding layer. 32. The method of claim 31, wherein the backless abrasive article comprises a fastener layer in direct contact with the adhesive layer. 33. An abrasive article formed from a cured formulation comprising a liquid polyoxyxene rubber, ceria reinforced particles, and abrasive particles. 34. The abrasive article of claim 33, wherein the ceria reinforced particles comprise fumed silica dioxide. 35. The abrasive article of claim 33, wherein the formulation comprises at least about 3 wt. The cerium oxide enhances the particles. 3. The abrasive article of claim 35, wherein the formulation comprises at least about 1% by weight of the cerium oxide enhancing particles. 37. The abrasive article of claim 33, wherein the abrasive particles are selected from the group consisting of nitrides, carbides, oxides, or blends thereof. </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> <RTIgt; 39. The abrasive article of claim 38, wherein the carbide is selected from the group consisting of carbonized smear, sinus, and carbonized. 4. The abrasive article of claim 39, wherein the carbide comprises carbon stone. 41. The abrasive article of claim 37, wherein the abrasive particles comprise a nitride. 42. The abrasive article of claim 41, wherein the nitride is selected from the group consisting of cubic boron nitride and tantalum nitride. 43. The abrasive article of claim 37, wherein the abrasive particles comprise an oxide. 44. The abrasive article of claim 43, wherein the oxide is selected from the group consisting of: dioxide dioxide, oxidized, oxidized, oxidized/oxidized, cerium oxide, oxidized, Rolling titanium oxide tin oxide, iron oxide and chromium oxide. 45. The abrasive article of claim 33, wherein the abrasive particles are selected from the group consisting of: cerium oxide, cerium &amp;&gt;, emulsified aluminum (melting or sintering), cerium oxide, zirconia /alumina, carbon 彳b &gt;, anaerobic garnet, diamond, cubic boron nitride, tantalum nitride, dioxide, 备 一 emulsified titanium 'titanium diboride, carbonization shed, tin oxide, carbonization Town, foundation # &quot; ^ titanium, iron oxide, chromium oxide, vermiculite, silicon carbide and any combination thereof. 46. The abrasive article of claim 33, wherein the formulation comprises at least about 30% by weight of the abrasive particles. 47. The abrasive particles of claim 44, wherein the abrasive article is wt%. Wherein the s-containing formulation comprises at least about 45. 48. The abrasive article of claim 47, wherein the scorpion. The furnish formulation comprises at least about 5 5 wt% of the abrasive particles. 49. The abrasive article of claim 33, wherein the liquid polyoxo rubber is formed from two 122813-990705.doc 1337915 partially polyoxyxene rubber, wherein the portion comprises a crosslinking agent. 50. The ground material of claim 49, wherein the crosslinking agent has a polyoxynium primary bond. The abrasive article of claim 33, wherein the cured formulation has an elongation at break of at least about 100%. The abrasive article of claim 5, wherein the elongation at break is at least about 120%. The abrasive article of claim 52, wherein the elongation at break is at least about 135%. Wherein the curing formulation has a Shore D hardness of no greater than wherein the curing formulation has no greater than the abrasive article having a tensile modulus of no greater than about 76, such as claim 33. The abrasive article of claim 33, having a tensile modulus of about 8.0 MPa. The abrasive article MPa of claim 5 5 is used. The abrasive article of claim 33, wherein the cured formulation has a tensile strength of at least about 7.0 MPa. The abrasive article of claim 33, wherein the tensile strength is at least about 7.5 MPa, such as the abrasive article of claim 33, wherein the abrasive article is in the form of a lapping plate and wherein the abrasive article has no backing. The abrasive article of claim 33, wherein the abrasive article is in the form of a plate having a major surface, wherein the major surface has a combination of surface protrusions. The abrasive article of claim 60, wherein the combination of surface protrusions is arranged in a pattern of J22813-990705.doc I337915. 62. The surface of the abrasive article of claim 61 is raised. 63. The surface of the abrasive article of claim 61 is raised. Wherein the surface protrusions such as "Hai" are inclined to the side walls, wherein the surface protrusions are vertical as the side of the object of claim 33, and the step further comprises an adhesive layer β 65, 如請求項33之研磨物件’其進一步包括適合於在一卡鉤 及環圈系統中連接之層。 66. 如請求項33之研磨物件,其中該固化調配物形成一具有 不大於約500密耳之厚度之層。 67‘如請求項66之研磨物件,其中該厚度係不大於約35〇密 耳。 68. —種方法,其包含: 摻合液體聚矽氧橡膠、二氧化矽增強顆粒及研磨粒以 形成調配物; 由該調配物形成一表面特徵層:及 使該調配物固化。 69.如請求項68之方法,其中使該調配物固化包括使該調配 物熱固化。 70·如請求項68之方法,其中使該調配物固化包括使用光化 輻射使該調配物固化。 71·如請求項68之方法,其中形成該表面特徵層包括在該表 面特徵層中形成一組表面結構,該等表面結構係經組態 成使表面積隨著磨損而增加。 122813-990705.doc 1337915 士 -月长項68之方法’其中形成該表面層包括形成具有不 大於約500密耳之厚度之層。 ” 73 · —種研磨物件,其包含: -包含聚⑦氧#合劑及研磨粒之層,該層具有至少約 1 00%之伸長率。 74. —種研磨物件,其包含: -表面特徵層,其包含經组態成使表面積隨著磨損而 增加之第-外表面,該表面特徵層包含聚矽氧黏合劑及 研磨粒,該表面特徵層具有不大於約1〇〇密耳之厚度, 該表面特徵層具有不大於約⑽密耳之厚度該表:特 徵層係自行支撑; /接與該相對於該第一外表面之表面特徵層接觸之黏 者層,忒黏著層係形成該研磨物件之第二外表面,且 其中該研磨物件無背層。 75. —種研磨物件,其包含: 具有表面突起之層,該層包含以氧黏合劑及研磨 粒;且其中該研磨物件具有至少約2〇之光澤效能。 122813-990705.doc65. The abrasive article of claim 33, which further comprises a layer adapted to be joined in a hook and loop system. 66. The abrasive article of claim 33, wherein the cured formulation forms a layer having a thickness of no greater than about 500 mils. 67' The abrasive article of claim 66, wherein the thickness is no greater than about 35 mils. 68. A method comprising: blending a liquid polyoxyxene rubber, cerium oxide enhancing particles, and abrasive particles to form a formulation; forming a surface feature layer from the formulation: and curing the formulation. 69. The method of claim 68, wherein curing the formulation comprises thermally curing the formulation. 70. The method of claim 68, wherein curing the formulation comprises curing the formulation using actinic radiation. The method of claim 68, wherein forming the surface feature layer comprises forming a set of surface structures in the surface feature layer, the surface structures being configured to increase surface area with wear. 122813-990705.doc 1337915 The method of the month-month length item 68 wherein forming the surface layer comprises forming a layer having a thickness of no greater than about 500 mils. 73. An abrasive article comprising: - a layer comprising a poly 7 oxygen # mixture and abrasive particles, the layer having an elongation of at least about 100%. 74. An abrasive article comprising: - a surface feature layer Having a first-outer surface configured to increase surface area with wear, the surface feature layer comprising a poly-xylene adhesive and abrasive particles, the surface feature layer having a thickness of no greater than about 1 mil, The surface feature layer has a thickness of no more than about (10) mils. The surface layer is self-supporting; and the adhesive layer is in contact with the surface feature layer of the first outer surface, and the adhesive layer forms the a second outer surface of the article, and wherein the abrasive article has no backing layer. 75. An abrasive article comprising: a layer having a surface protrusion, the layer comprising an oxygen binder and abrasive particles; and wherein the abrasive article has at least A gloss performance of about 2 inches. 122813-990705.doc
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BRPI0714710A2 (en) 2013-03-26
WO2008008535A1 (en) 2008-01-17
KR20090029842A (en) 2009-03-23
US20130125474A1 (en) 2013-05-23
US8349041B2 (en) 2013-01-08
JP2009543705A (en) 2009-12-10
HK1136242A1 (en) 2010-06-25
CN102990530B (en) 2016-02-10
US20110232198A1 (en) 2011-09-29
JP2012250340A (en) 2012-12-20
JP5401311B2 (en) 2014-01-29
CA2661504C (en) 2013-04-23
TW200812755A (en) 2008-03-16
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US20080014840A1 (en) 2008-01-17
JP5529915B2 (en) 2014-06-25
CL2007002055A1 (en) 2008-01-11
AU2007272779A1 (en) 2008-01-17
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PL2079559T3 (en) 2013-03-29

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